State of Madhya Pradesh - Act
The Narcotic Drugs and Psychotropic Substances (Madhya Pradesh) Rules, 1985
MADHYA PRADESH
India
India
The Narcotic Drugs and Psychotropic Substances (Madhya Pradesh) Rules, 1985
Rule THE-NARCOTIC-DRUGS-AND-PSYCHOTROPIC-SUBSTANCES-MADHYA-PRADESH-RULES-1985 of 1985
- Published on 11 November 1985
- Commenced on 11 November 1985
- [This is the version of this document from 11 November 1985.]
- [Note: The original publication document is not available and this content could not be verified.]
Chapter I
Preliminary
1. Short title and commencement.
2. Definitions.
- In these rules, unless the context otherwise requires :-Chapter II
Opium Rules
3. Licence to Medical Practitioner.
4. Licence to Druggist.
5. Permit to person addicted.
6. Renewal of Licence or Permit.
7. Import inter-State, Export inter-State or transport.
8. Transmission by post.
9. Sale.
- Opium shall not be sold at any place except at a Government ware-house, Treasury or sub-treasury of the State of Madhya Pradesh :Provided that an approved medical practitioner or a druggist holding a licence in Form O.P. 1 or O.P. 2 may sell medicines containing opium or preparations containing opium to the extent and subject to the conditions laid down in his licence.10. Supplementary directions by the Excise Commissioner.
- Subject to the provisions of the Act and these rules the Excise Commissioner may from time to time give such directions and prescribe such returns and register, as he may think fit for the purposes of carrying out the provisions of these rules.11. Exemptions granted to Government Servants.
- Government Servants, when acting on behalf of the Government and in the course of their duties as such are exempted from the provisions regarding the import inter-state export inter-state, transport, possession and sale of opium or its transmission by inland post.12. Exemption granted to Hospitals and Dispensaries.
- The following hospitals and dispensaries are exempted from the provisions regarding possession and sale of opium as defined in Section 2 of the Act, in so far as 'Sale' consists in taking payment for medicines issued in accordance with the rules prescribed for the hospitals or dispensaries, concerned ;-13. All articles or things confiscated to be delivered to the District Excise Officer.
14. Disposal to be deferred till period of appeal.
- The sale or other disposal of any thing or any animal confiscated under the Act shall be deferred until the period of appeal against the order of confiscation has expired or if an appeal be made against such order, until such appeal has been decided :Provided that any perishable thing or any animal may be disposed of immediately.15. Reward to be paid to officers and informers.
| (i) | On first 10 Kg. of opium | up to Rs. 40 per Kg |
| (ii) | On next 30 Kg. of opium | up to Rs. 30 per Kg |
| (iii) | On excess of 40 Kg. of opium | up to Rs. 20 per Kg |
| (i) | On first 20 Kg. of opium | Non-information cases up to Rs. 40 per Kg. | Information cases up to Rs. 30 per Kg. |
| (ii) | On excess of 20 Kgs. of opium | Up to Rs. 30 per Kg. | Up to Rs. 20 per Kg. |
| (i) | District Excise Officer | Up to Rs. 100 in each case. |
| (ii) | Collectors | Up to Rs. 500 in each case. |
| (iii) | Divisional Assistant Commissioner of Excise | Up to Rs. 300 in each case. |
| (iv) | Divisional Deputy Commissioner of Excise | Up to Rs. 500 in each case. |
| (v) | Excise Commissioner | Up to Rs. 2000 in each case. |
| (vi) | The State Government | Above Rs. 2000 in each case. |
Chapter III
Narcotic Drugs Rules
16. Manufacture.
- A Licensed vendor or licensed druggist may, subject to the conditions of his licence, manufacture medicinal opium or any preparation containing morphine, diacetyl-morphine or cocaine from materials which he is lawfully entitled to possess.17. Manufactured by approved medical practitioners and Government officers exempted.
- Approved medical practitioners in the exercise of their profession and officers of Government, who in the course of their official duty or for the purposes of such duty, are required to manufacture medicinal opium or any preparation containing morphine, diacetyl-morphine or cocaine shall be exempted from the provisions contained in these rules regarding manufacture.Possession18. Possession by private person.
- Any person may possess such quantity of manufactured drugs other than prepared opium as has been at one time dispensed and sold for his use on the prescription of an approved medical practitioner :Provided that the prescription is in writing, elated and signed by an approved medical practitioner with his full name and address, states the exact quantity of each manufactured drug, gives the full name and address of the person for whose use it is given, and is in the possession of such person or his guardian a person duly authorised on his behalf.19. Possession by approved medical practitioner.
- An approved medical practitioner may possess for his use, in the exercise of his profession, manufactured drugs other than prepared opium in quantities not exceeding in the aggregate those specified below :-| Description of Drugs | Quantity | |
| (1) | (2) | |
| (i) | Cocaine | 14,175 Mgs. |
| (ii) | Medicinal hemp | 2,83,500 Mgs. |
| (iii) | Medicinal Opium | 2,83,500 Mgs. |
| (iv) | Morphine, diacetyl-morphine and admixtures ofalkaloids of these drugs. | 7,700 Mgs. of pure drugs or 2,26,800 Mgs. of thesedrugs in all forms of admixture of alkaloids. |
| (v) | Pethidine Hydrochloride | 72,00 Mgs. |
20. Possession by licensed vendor or licensed druggist.
- A licensed vendor or licensed druggist may possess such quantity of coca leaf and manufactured drugs other than prepared opium and in such manner as may be specified in his licence.21. Exemption.
- The following institutions shall be exempted from the provisions contained in these rules regarding the possession of coca leaf and manufactured drugs [other than prepared opium and morphine] [Substituted by Notification No. (37)-B-1-73-99-CTD-V, dated 14-5-1999.] ;-22. Import by private persons.
- Any person may import inter-state such manufactured drugs other than prepared opium as he may lawfully possess under Rule 18.23. Import by others.
| Cases in which licence may be granted | Authority granting the licence | |
| (1) | (2) | |
| (i) | For supplies required for hospitals,dispensaries and veterinary dispensaries working under Governmentsupervision, subsidized dispensaries and railway hospitals anddispensaries. | The indent shall be counter-signed by theDirector of Health Services, Director of Veterinary Services,District Surgeon of the Railway Administration concerned as thecase may be. This indent shall be regarded as a licence. |
| (ii) | Other medical institutions specially authorisedby the Excise Commissioner | The indent shall be counter-signed by the CivilSurgeon of the district and such indent shall be regarded as alicence. |
| (iii) | In all other cases | The Collector of the District. The licence shallbe in Form N.D. 3. |
24. Import subject to restrictions specified in the import licence.
- A person to whom a licence has been granted under these rules for the import of coca leaf and manufactured drugs other than prepared opium shall import only such quantity and in such manner as may be specified in his licence.25. Export.
- To Export Inter-State coca leaf and manufactured drugs other than prepared opium, may be permitted by the Excise Commissioner under a licence in Form N.D. 3, such licence shall not be granted except on the production of an import licence, issued by an officer duly authorised in that behalf by the Government of the importing State.26. Transit.
- A licence in Form N.D. 3 for the transit of coca leaf and manufactured drugs other than prepared opium consigned to any other State through Madhya Pradesh may be granted by the Excise Commissioner on application by the Chief Excise authority of that State. The articles shall be carried in sealed packages and shall not be opened en route.27. Transport.
- A licence for the transport of coca leaf and manufactured drugs other than prepared opium within the limit of possession authorised may be granted by the following authorities :-| Cases in which licence may be granted | Authority granting the licence | |
| (1) | (2) | |
| (i) | For supplies required for hospitals,dispensaries and veterinary dispensaries working under Governmentsupervision, subsidized dispensaries and railway hospitals anddispensaries. | The indent shall be counter-signed by theDirector of Health Services, Director of Veterinary Services,District Surgeon of the Railway Administration concerned as thecase may be. This indent shall be regarded as a licence. |
| (ii) | Other medical institutions specially authorisedby the Excise Commissioner | The indent shall be counter-signed by the CivilSurgeon of the district and such indent shall be regarded as alicence. |
| (iii) | In all other cases | The Collector of the District. The licence shallbe in Form N.D. 3. |
28. Transmission by post.
- Import Inter-state Export Inter-state or transport of coca leaf and manufactured drugs other than prepared opium by inland post is prohibited, except by licensed druggist and licensed vendors and shall be subject to the following conditions :-29. Licence of sale.
| Licence for the Sale of | Quantity allowed and licence fee payable for | ||||
| Druggist/s Licence | Vendor/s Licence | ||||
| Quantity | Rs. | Quantity | Rs. | ||
| (1) | (2) | (3) | (4) | (5) | |
| (i) | Coca derivatives and cocaleaf | 28,353 mgs. | 10.00 | 56,700 mgs. | 5.00 |
| (ii) | Medicinal Hemp- | ||||
| (a) Extract of hemp | 4,25,250 mgs. | 2.00 | 56,700 mgs. | 1.00 | |
| (b) Tincture of hemp | 4,252,500 mgs. | 2.00 | 5,67,000 mgs. | 1.00 | |
| (iii) | Medicinal opium or | 4,25,250 mgs. | 10.00 | 5,67,000 mgs. | 5.00 |
| Tincture opium | 4,252,250 mgs. | 10.00 | 5,670,000 mgs. | 5.00 | |
| (iv) | Morphine diacetyl-morphine or official or non-officialpreparations containing more than 0.2 per cent of morphine orcontaining any diacetyl-morphine | 15,440 mgs. of pure drugs or 226,800 mgs. of these drugs inall forms of admixtures of alkaloids. | 10.00 | 15,400 mgs. of pure drugs or 226,800 mgs. of these drugs inall forms of admixtures of alkaloids. | 5.00 |
| (V) | Pethidine Hydrochloride | 144,000 mgs. | 10.00 | 144,000 mgs. | - |
30. Sale by a licensed vendor.
- A licensed vendor may subject to the conditions of his licence sell only to the following persons :-31. Sale by a licensed druggist.
- A licensed druggist may subject to the conditions of the licence, sell only on prescription of approved medical practitioners such coca leaf or manufactured drugs other than prepared opium as may have been allowed in his licence. He shall maintain a written record of every such sale as laid down in his licence and as ordered by the Excise Commissioner from time to time.32. Exemption.
33. Additional account returns to be maintained by others.
- The importer of manufactured drugs, the manufacturer of drugs, and the Chemist and Druggist shall maintain the registers of accounts, returns etc. in forms N.D. 7, N.D. 8 and N.D. 9 respectively.34. Stock of drugs to be made over to Collector on expiration, cancellation or suspension of a licence or order.
- On the expiration, cancellation or suspension of any licence granted or any order passed under these rules, the holder thereof shall forthwith make over the Collector all manufactured drugs anil coca leaf in his possession and shall, with the prior sanction of the Collector, dispose of these drugs to any other person authorised to possess them under these rules or under rules for the time being in force in any part of India within two calendar months from the date of such expiration, cancellation or suspension of the licence or order. If the Collector so directs, the drugs made over to him as aforesaid shall be sealed by an officer appointed by hint that behalf and shall be kept in the custody of the holder until they are disposed of.35. Disposal of drugs deposited on cancellation of licence.
- The Collector shall, if necessary cause all coca leaf and manufactured drugs other than prepared opium delivered to him under Rule 34 to be examined by the Chemical examination or by such other officer as the Excise Commissioner may direct.36. Provisions not to apply to certain substances.
- The provisions of these rules shall not apply to the importation, exportation, transportation, possession or sale of codeine, dionin and their respective salts, unless the quantity involved in any transaction or possession at any one lime exceeds 450 grams.37. Supplementary directions by the Excise Commissioner.
- Subject to the provisions of the Act and these rules the Excise Commissioner may, from time to time, give such directions and prescribe such forms, returns and registers as he may think fit, for the purpose of carrying out the provisions of these rules.[Chapter III] [Inserted by Notification No. 1818-B-1-67-V-SR-85, dated 23-4-1986.] A Poppy Straw Rules37A. Prohibition of Poppy straw.
- Save as provided in these rules the possession, transport, import inter-state, Export inter-State, Warehousing, sale, purchase, consumption and use of poppy straw is prohibited, except for medical or scientific purposes in the manner and to the extent provided by the provisions of the Act and the rules and orders made there under and also in accordance with the terms and conditions of the licence, or permit granted or authorisation made under the provisions of this Chapter.[Proviso... Omitted] [Omitted by Notification No. (36)-B-1-1-05-2-V, dated 11-10-2007.]37B. Depots for sale of poppy straw.
- Depots for the sale of poppy straw shall be established at such places as the Excise Commissioner, may from time to time direct. Poppy straw required for sale at a depot may be obtained from such place or places as the Excise Commissioner may direct.37C. Declaration by cultivator of opium poppy.
- The cultivator licensed under Section 9 of the Act shall in each financial year submitted by the 1st April to the District Excise Officer of the area a true declaration in Form P.S. I, in respect of the land in which he cultivated the opium poppy and of the stocks of Poppy straw directly relatable to the crop produced by him and shall also declare every building or place used or to be used by him for storing the poppy straw.37D. [ Sale of poppy straw. [Substituted by Notification No. (34)-B-1-58-96-CTD-V, dated 29-8-1996.]
- (i) No person shall sell poppy straw except under a wholesale licence granted in Form P.S. II and P.S. II-A or a retail sale licence in Form P.S. Ill for Medical or Scientific purposes.37E. Licensing authority and licence fee.
- [(1) Licences in Form P.S. II and P.S. Ill shall be granted by auction or tender or on fixed annual licence fee for the financial year or a part thereof by the Collector for the area within his jurisdiction, subject to the terms and conditions issued by the Excise Commissioner.] [[Substituted by Notification No. (10)-B-1-4-2002-CTD-(V), dated 23-4-2002. Prior to substitution it was as under :'(1) Licences in Form P.S. II and Form P.S. Ill shall be granted by auction or tender by the Collector for the area within his jurisdiction, subject to the terms and conditions approved by the Excise Commissioner.']]37F. Import inter-state.
- A licensee holding licence in Form P.S. II only may import inter-state poppy straw in accordance with a pass granted by the licensing authority, or any Officer duly authorised by him. [The pass for import inter-state shall be issued in Form IV after payment of import fee at the rate of rupees 10 per kilogram] [Substituted by Notification No. (50) B-1-70-99-CTD-V, dated 15-10-1999.],37G. Export inter-state.
37I. Place of sale by licensee.
- A licensee holding a licence in form [P.S. II or P.S. II-A] [Substituted by Notification No. (34) B-1-58-96-CTD-V, dated 29-8-1996.] or in Form P.S. Ill shall not effect sales of poppy straw at any place or premises other than the place or the premises specified in his licence.37J. Bonds for performance of conditions of licence.
37K. Production of licence and accounts.
- The licensee holding the licence under this chapter shall at once produce his licence and accounts for inspection on demand by any officer appointed under Section 7of the Act and he shall not prevent any such officer from entering the place or premises mentioned in this licence at any hour during day or night.37L. Furnishing of returns.
- The licensee holding a licence under this chapter shall furnish such returns and information as may from lime to time be required by the licensing authority.37M. Disposal of balance.
- The following conditions shall apply to the disposal of balance of poppy straw left with a licensee holding a licence under this Chapter after cancellation or determination of his licence ;-37N. Restriction on Railway Authority or Transport Agency.
- No Railway authority or Transport Agency shall :-37O. Medical use of poppy straw.
37P. The manner in which a Certificate may be issued by the Medical Officer.
- The Medical Officer of the district, where addict of poppy straw resides, shall follow the procedure prescribed in this rule for the exemption of a person applying for a permit for the possession of poppy straw for personal consumption on medical grounds and for the issue of a certificate to him (hereinafter called the applicant) :37Q. Poppy Straw for Scientific Purpose.
37R. Renewal of Licence/Permit.
37S. [ Transit allowance. [Inserted by Notification No. (23)-B-1-19-2000-CTD-V, dated 30-3-2000.]
37T. [ Storage loss and margin of deviation. [Inserted by Notification No. (23)-B-1-19-2000-CTD-V, dated 30-3-2000.]
37U. [ Limitation of prosecution. [Inserted by Notification No. (25) B-1-1-05-2-V, dated 31-3-2006.]
- No Court shall take cognizance of an offence against a licensee of poppy straw in wholesale or retail, for the breach of the conditions of licence, pass or permit issued under Narcotic Drugs and Psychotropic Substances (Madhya Pradesh) Rules, 1985 and punishable under the Narcotic Drugs and Psychotropic Substances Act, 1985 and the Narcotic Drugs and Psychotropic Substances (Madhya Pradesh) Rules, 1985 except on a complaint, report or sanction of the Collector of the Distrcit concerned.]Chapter IV
38. Appeal.
- An appeal shall lie from an original or appellate order of an Excise Officer as follows, namely :-39. Limitation of Appeal and Copy of order objected to accompany petition.
40. Power of Appellate Authority.
41. Power to stay execution of orders.
42. When the appeal shall be final.
43. Power of revision of Superior Officers.
- The Chief Revenue Authority or the Excise Commissioner or the Collector may, at any time on its/his motion or on the application made by the party for the purpose of satisfying itself or himself as to the legality or propriety of any decision made up order passed by any officer subordinate to it or him call for and examine the record of any case pending before or disposed of by such officer, and may pass such order in reference thereto, as may appear proper :Provided that-44. Application for revision.
- An application for revision shall be presented in the same manner as a petition of appeal.45. No appeal against certain order.
- No appeal shall lie from tiny order rejecting an application for revision.46. Transfer of appeals or applications for revision.
- The State Government may transfer any appeal or application for revision from the Excise Commissioner or a Collector to any officer specially authorised to dispose of such appeals or application under clause (c) or clause (d) of Rule 2 of rules of chapter I.47. Authority/Officers to whom revision lies.
- Any order passed by an excise officer may be revised by the State Government, the Excise Commissioner or the Collector to whom such officer is subordinate under these rules either on its or his own motion, or on the application of any person or party interested and in the latter case such application shall be presented in the same manner as memorandum of appeal.[Chapter IV-A] [Inserted by Notification No. (37I-B-1-73-99-CTD-V. dated 14-5-1999.]47A. Special provisions relating to use etc. of morphine by the recognised medical institutions.
- Notwithstanding any provision to the contrary contained in these rules, possession, transport, purchase, sale, import inter-state, export inter-state or use of morphine or any preparation containing morphine in respect of or by a recognised medical institution, shall be as per the provisions of this chapter.47B. Definitions.
- In this chapter, unless the context otherwise requires :-47C. Recognition of medical institutions and cancellation thereof.
47D. Duties of recognised medical institution.
- Every recognised medical institution shall-47E. Sending of estimates of requirement of morphine by the recognised medical institution.
- Every recognised medical institution shall send their annual requirement of morphine in Form M-3 by 30th November of the preceding year alongwith the name and address of the supplier from whom they intend to buy it, to the Drug Controller.47F. Approval of estimates by the Drug Controller.
- The Drug Controller on receipt of estimates of the annual requirement shall consider it, and may, if necessary, call for necessary clarifications. A reply regarding approval or non-approval thereof shall be sent before the 21st of December of the preceding year. A copy of the communication shall be sent to each supplier whose name has been given in the estimate, if the supplier is located in another State thereto the Drug Controller of that State, the Drug Controller General of India and the Narcotics Commissioner of India.47G. Supplementary estimates.
- If the requirement of the recognised medical institution exceeds the annual estimate approved by the Drug Controller, the recognised medical institution may send a supplementary estimate at any time to the Drug Controller which shall be considered and dealt with by the Drug Controller in the same manner as prescribed for the annual estimates.47H. Possession, transport, sale, import inter-state etc. of morphine.
- Possession, transport, purchase, sale, import inter-state, export inter-State or use of morphine in respect of or by a recognised medical institution shall be regulated in accordance with the following provisions :-47I. Maintenance of Records.
- All records generated under this chapter shall be kept for a period of two years from the date of transaction which shall be open for inspection by the officers empowered by the State Government under Sections 41 and 42 of the Act.47J. Inspection of stocks of morphine.
- The stocks of morphine under the custody of a recognised medical institution shall be open for inspection by the Drug Controller or any other officer subordinate to him or other officers of the State Government empowered under Sections 41 and 42 of the Act, and the rules made thereunder.47K. Appeals.
- Any institution aggrieved by any decision or order passed by the Drug Controller relating to recognition, revocation of recognition of any institution or non-approval or cancellation of approval of estimates may appeal to the Secretary. Public Health and Family Welfare Department within ninety days from the date of communication of such decision or order.]Chapter V
General
48. Period of licence or permit.
- No licence or permit under the aforesaid provisions shall be granted for any period beyond 31st March, next following the date of commencement of the licence or permit as the case may be.49. The personal character of the Licensee.
- Every licence granted under these rules shall be deemed to have been granted personally to the licensee named therein and shall, on the expiry thereof, be surrendered to the District Excise Officer. If any licence holder dies during the currency of his licence such licence shall forthwith cease to be in force.49A. [ [Inserted by Notification No. (50)-B-1-70-99-CTD-V, dated 15-10-1999.]
No agent or servant shall be appointed by any licensee for the management of any licence or operations connected therewith, without previous approval of the District Excise Officer.]50. Cancellation of licence or order.
- Subject to any directions that the Excise Commissioner may give in this behalf, the officer who has granted a licence or has by order approved or authorised, any person under these rules, may cancel or suspend such licence or order :-51. Repeal and Savings.
1. This licence shall remain in force from ........ to ...... (both days inclusive).
2. The licensee shall not have in his possession at any one time medicines containing opium exceeding............
3. The licensee may obtain his requirements of medicines containing opium from any licensed druggist or manufacturer licensed under the provisions of the Medical and Toilet Preparations (Excise Duties) Act, and rules made thereunder who is permitted to sell such medicines under the Madhya Pradesh Narcotic Drugs and Psychotropic Substances Rules, 1985, or may import the same from any other part of India subject to the provisions of the said rules.
4. The licensee shall not dispense any medicine containing opium for his patients except under a prescription issued by him and in the manner laid down in such prescription.
5. The licensee shall not keep medicines containing opium except at his dispensary.
6.
| Date | Opening balance | Quantity received this day and when received | Total quantity to be accounted | Quantity sold this day |
| (1) | (2) | (3) | (4) | (5) |
| Full name of Purchaser | Full address | Date of prescription with name of approvedmedical practitioner who granted. | Balance | Remarks |
| (6) | (7) | (8) | (9) | (10) |
7. This licence may be suspended or cancelled at any time by the officer granting it,-
8. In case this licence is surrendered or cancelled during the currency of the period for which it is granted or is not renewed on its expiry a licensee shall forthwith handover the whole of the stock of medicines containing opium to the Collector. The licensee shall also handover to the Collector all accounts passes and prescriptions in original which he is required to keep and preserve under this licence.
Granted this............day of.......19.........................Seal of the office.Place.........Signature and designation of theOfficer granting the licence.Form O.P.-21. The licensed druggist shall-
| Date | Opening balance | Quantity received this day and when received | Total quantity to be accounted | Quantity sold this day |
| (1) | (2) | (3) | (4) | (5) |
| Full name of Purchaser | Full address | Date of prescription with name of approvedmedical practitioner who granted. | Balance | Remarks |
| (6) | (7) | (8) | (9) | (10) |
2.
3. In case this licence is surrendered suspended or cancelled during the currency of the period for which it is granted or is not renewed on its expiry the licensee shall forthwith handover the whole of the unused stock of the medicines or preparations containing opium to the Collector. The licensed druggist shall also handover to the Collector all accounts, passes and prescriptions in original which he is required to keep and preserve under this licence.
4. The licence may be withdrawn at any time without notice at the discretion of the Collector.
Granted this..............day of.......... 19...Seal of OfficeCollectorDistrictForm O.P 3[See Rule 5 (2)]Form of Register of Opium Addicts| S. No. | Full name of the Addicts | Age | Religion |
| (1) | (2) | (3) | (4) |
| Caste | Place of residence with tehsil | Period for which addicted to opium | Name of the ailment, etc. for which opium isrequired |
| (5) | (6) | (7) | (8) |
| Quantity of opium required per month | Quota of opium sanctioned by the medicalauthority | Permit No. and date with designation of themedical authority. | Remarks. |
| (9) | (10) | (11) | (12) |
1. This permit shall remain in force from.................. to .............. (both days inclusive).
2. The permit-holder shall as soon as possible present this permit before the Excise Sub-Inspector of his circle or area for his counter-signature and in any case not later than one month of the receipt of this permit.
3. The opium purchased under this permit shall be used solely for the personal consumption by the permit-holder and he is not entitled to transfer it to others.
4. The permit-holder shall not purchase during any one month opium exceeding provided that this quantity may be reduced during the currency of the permit.
5. Opium will be issued to the permit-holder in each quarter as under :-
| Period | Monthly quota |
| April to June | ......................................grams |
| July to September | ......................................grams |
| October to December | ......................................grams |
| January to March | ......................................grams |
6. The permit shall obtain his supplies of opium from................... warehouse/treasury/sub-treasury only. The permit-holder shall get the details of each purchase entered on the reverse of the permit by the officer issuing opium before he removes the opium purchased by him from the premises.
7. The permit-holder shall credit the price of opium at such rale as may be fixed by Government, from time to time in this behalf in a treasury or sub-treasury and shall present the receipted treasury challan to the officer-in-charge for issuing opium.
8. This permit shall be personal and non-transferable, and may be cancelled at any time by the officer granting it.
9. On breach of any of the above conditions, or provisions of the Narcotic Drugs and Psychotropic Substances Act, 1985, and rules made thereunder or of any executive orders or instructions, issued from time to time this permit shall he cancelled.
Granted this............ day.....................of.................19................................................Signature or left-hand thumbimpression of the permit-holder..................................Signature and designation of officer granting the permit...................................Countersigned Inspector/ Sub-Inspector (Excise)................................................ CircleDated 19..........(Reverse of the Permit)Details of each purchase of opium made by the permit-holder from.............. to ................19................| Date | Total quantity of opium permitted to be purchasedin current month | Quantity of opium purchased | Total quantity of opium purchased in the currentmonth | Difference of column (2) and (4) | Signature of the officer in-charge issuing opium. |
| (1) | (2) | (3) | (4) | (5) | (6) |
| Description of drugs | Quantity or weight | Packages |
| (1) | (2) | (3) |
| Description of drugs | Quantity weight | Packages |
| (1) | (2) | (3) |
| Date | Quantity of drug held in stock | Particulars of import certificate | Particulars of licence issued if any |
| (1) | (2) | (3) | (4) |
| Particulars of Export Authorization issued by thecountry of origin | Quantity received | From whom received | |
| Name | Address | ||
| (5) | (6) | (7) | (8) |
| Total Cols. (2) & (6) | Quantity issued for manufacture | Balance | Remarks |
| (9) | (10) | (11) | (12) |
| Date | Quantity of the drug received for manufacture | Form in which manufactured and quantity of drugin unit | Anticipated theoretical yield | Actual yield | Wastage if any and disposal of wastage | Quantity transferred to record of sales |
| (1) | (2) | (3) | (4) | (5) | (6) | (7) |
| Drugs manufactured and transferred to stores | Total | Initial of person in charge of manufacturingoperations. | |||
| Ampules No. Quty. | Tablets capsules No. Quty. | Powder Qty. Conc. | Liquid preparation Qty. Conc. | ||
| (8) | (9) | (10) | (11) | (12) | (13) |
| Date | Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Total |
| (1) | (2) | (3) | (4) | (5) | (6) |
| Quantity of drug received for sale frommanufacturing department | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Total |
| (7) | (8) | (9) | (10) | (11) |
| Total Stock | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Quantity of drug (Cols. 6+11) |
| (12) | (13) | (14) | (13) | (16) |
| Quantity sold | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Total quantity of the drug sold |
| (17) | (18) | (19) | (20) | (21) |
| To whom sold | |||
| Name | Address | Authority for sale | Mode of delivery |
| (22) | (23) | (24) | (25) |
| Closing balance | Initials of the persons making the entry | Remarks | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Total quantity of drug | ||
| (26) | (27) | (28) | (29) | (30) | (31) | (32) |
1. You shall not transfer this licence to any other person.
2. You shall not have in your possession more than miligrams of [.............] [Here enter the kind of the drugs that may be sold e.g. (1) coca derivatives and coca leaf, (2) medical hemp, (3) medical opium or (4) morphine diacetyl-morphine or official or non-official preparations containing more than 0.2 per cent of morphine or containing any diacetyl-morphine, as the case may be.]and other allied drugs taken together.
3. You shall not sell [..............] [Here enter the kind of the drugs that may be sold e.g. (1) coca derivatives and coca leaf, (2) medical hemp, (3) medical opium or (4) morphine diacetyl-morphine or official or non-official preparations containing more than 0.2 per cent of morphine or containing any diacetyl-morphine, as the case may be.] except on the premises for which this licence is granted.
4. You shall not sell [.......] [Here enter the kind of the drugs that may be sold e.g. (1) coca derivatives and coca leaf, (2) medical hemp, (3) medical opium or (4) morphine diacetyl-morphine or official or non-official preparations containing more than 0.2 per cent of morphine or containing any diacetyl-morphine, as the case may be.] except to the following persons in quantity not exceeding what they may respectively lawfully possess :-
5. You shall maintain correct account of transactions in the following form, a separate page being set-aside for each different preparation of the drug :-
| Date | Opening balance | Quantity received this day and whence received | Total quantity to be accounted for |
| (1) | (2) | (3) | (4) |
| Quantity sold this day | Full name of purchaser | Full Address | Balance | Remarks |
| (5) | (6) | (7) | (8) | (9) |
6. You shall file ail import passes properly.
7. You shall produce your licence, file of passes and account book and your stock for inspection immediately on demand of any officer specially of generally authorised by the Collector or any officer not below the rank of Sub-Inspector of Excise or police or of Naib Tahsildar. In support of the receipt you shall produce the permits and invoices of supplies obtained.
8. This licence may be cancelled by the Collector if any breach of any of the provisions of the Narcotic Drugs and Psychotropic Substances Act, 1985 (No. 61 of 1985) or of the rules made thereunder or of the above mentioned conditions is committed by you or by any persons employed by you on the premises for which this licence is granted.
Dated......... 19...Collector............District.Form N.D. 2(See Rule 29)Licence for the Sale of Coca Leaf and Manufactured Drugs other than Prepared Opium by a DruggistUnder Rule 29 of the Narcotic Drugs and Psychotropic substances Rules, Madhya Pradesh, 1985 and in consideration of the payment of a fee of Rs......... the receipt of which is hereby acknowledged licence is hereby granted to you..............druggist to sell...............bona fide as medicine from your premises in............street in the town of..................in the district of...................during the year ending the 31st March 19... subject to the following conditions, namely :-Conditions1. You shall not transfer this licence to any other person.
2. You shall not have in your possession at any one time more than miligramme of [..............] [Here enter the kind of the drugs that may be sold e.g. (1) coca derivatives and coca leaf. (2) Medical hemp, (3) medical opium or (4) morphine diacetyl-morphine or official or non-officiai preparations containing more than 0.2 per cent of morphine or containing any diacetyl-morphine, as the case may be.]
3. You shall not sell except on the premises for which this licence is granted.
4. You shall obtain the drugs to be sold under this licence from a licensed vendor thereof in India and you shall not receive or have in your possession any such drugs obtained otherwise.
5. You shall not sell to any person other than a person producing the prescription of an approved medical practitioner and not exceeding such quantity as may be entered in such prescription.
6. You shall not sell coca leal or the manufactured drugs specified above unless the prescription is in writing, is dated, is signed, by an approved medical practitioner with his full name and address and give the full name and address of the person for whose use it is given. You shall not sell more than once on the authority of a prescription unless it contain a superscription by an approved medical practitioner stating that it is to be repeated, the intervals at which it is to be repeated and the number of limes it is to be repealed.
7. You shall retain ever)' prescription on the authority of which you sold the drug :
Provided that you shall first warn the person presenting the prescription that unless it bears a superscription as aforesaid it will be retained and not repeated.8.
9. You shall not store any manufactured drug or coca leaf to be sold under this licence in any premises other than those named herein.
10. You shall keep a correct account in the following form, to be balanced at the close of each day a separate set of pages being set-aside for each different preparation of the drug stocked by you :-
| Date | Opening balance | Quantity receivedthis day and whence received | Total quantity to beaccounted for | Quantity sold thisday |
| (1) | (2) | (3) | (4) | (5) |
| Full name of purchaser | Full Address | Date of prescription and name of approved medicalpractitioner who issued it | Balance | Remarks |
| (6) | (7) | (8) | (9) | (10) |
11. (a) You shall produce your licence, the accounts of sale of coca leaf or the manufactured drugs specified in his licence, the file of prescription and your stock for inspection immediately on the demand of any officer specially or generally authorized by the Collector or any officer not below the rank of sub-inspector of excise or police or of Naib Tahsildar. In support of the receipts you shall produce the permits and invoices of supplies obtained and in support of the issue the prescription on which the drugs were sold.
12. This licence may be cancelled by the Collector if any breach of the Narcotic Drugs and Psychotropic Substances Act, 1985 (No. 61 of 1985) or of the rules made thereunder or of the above mentioned conditions is committed by you or your partner or agent or any other person employed by you on the premises for which this licence is granted.
CollectorDated.....19...District.Form N.D. 3Form of licence for the import interstate/export interstate/transport/transit of [............] [Here enter the kind of drug allowed to be imported/exported/transported, e.g. (1) coca derivatives and coca leaf, (2) medicinal help, (3) medicinal opium, or (4) morphine, diacetyl-morphine (official or non-official preparations) as the case may be. They should be entered on the licence and the duplicate and triplicate copies thereof also.](To be issued in quadruplicate. One copy being kept as a counterfoil in the office of issue, another to be returned by the consignor to the Collector of the district to which the consignment is sent after noting the details of the drugs consigned on the form on the back of the foil, the third to be sent to the authority of the exporting district and the fourth to accompany the consignment).Licence granted to..............(here enter name of consignee) to import interstate from/export interstate to/transport from or via (here enter locality and district) into/from/ to (here state district) manufactured drugs other than prepared opium coca leal to the amount of....................... as specified below :-(here state description and weight or quantity of each kind of drug).This licence must he used within one month From the date of its issue. The duplicate shall he returned by the consignor after despatch of the consignment to the Collector............(here enter district).The Bulk of the consignment shall not he broken in transitPlace ........Date ................Excise Commissioner/CollectorForm N.D. 3DuplicateForm of licence for the import interstate/export interstate/transport/transit of .....(Here enter the name of drug)(To he returned by the consignor to the Collector of the district to which the consignment is sent after noting details of the drugs consigned in the form on the back of this foil).Licence granted to...........(here enter name of consignee) to import interstate from/export interstate to/transport from or via .......... (here enter locality and district) into/from/to ........... (here state district) manufactured drugs other than prepared opium coca leaf to the amount of as specified below :-(here state description and weight or quantity of each kind of drug).This licence must he used within one month from the date of its issue. The duplicate shall be returned by the consignor after despatch of the consignment to the Collector................... (here enter district).The bulk of the consignment shall not be broken in transit.Place.......Date.........Excise Commissioner/CollectorForm overleaf to be filled up, signed and dated by the consignor and this duplicate to be returned to Collector........Backside of 'Duplicate' of Form N.D. 3Details of ConsignmentThe drugs specified below have this day ....... 19 ... been despatched by ........ (mode of conveyance) incharge of....... in ......... (state No. and description of packages)| Description of drugs | Quantity or weight | Packages |
| (1) | (2) | (3) |
| Description of drugs | Quantity or weight | Packages |
| (1) | (2) | (3) |
| Date | Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. |
| (1) | (2) | (3) | (4) | (5) |
| Quantity of the drug received | Dealer or firm from whom received | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Name | Address |
| (6) | (7) | (8) | (9) | (10) | (11) |
| Total | Patient's | ||||
| Ampules No. Qty. | Tablets capsules No. Qty. | Powder Qty. conc. | Liquid preparation Qty. conc. | Name | Card No. |
| (12) | (13) | (14) | (15) | (16) | (17) |
| Total daily dose | Administered by | Physician | Closing balance | |||
| Ampules No. Qty. | Tablets capsmes. No. Qty. | Powder Qty. conc. | Liquid preparation Qty, conc. | |||
| (18) | (19) | (20) | (21) | (22) | (23) | (24) |
| Date | Drug in stock | Drug received | ||
| from | Quantity | from | Quantity | |
| (1) | (2) | (3) | (4) | (5) |
| from whom received | Total quantity | Patients | ||||
| Name | Address | from | Name | Address | Disease | |
| (6) | (7) | (8) | (9) | (10) | (11) | (12) |
| Card No. | Quantity of the drug used during the day on eachpatients | Closing balance | Signature of the Registered Medical Practitioner | Remarks |
| (13) | (14) | (15) | (16) | (17) |
1. Full name of the patient......................................... ......
2. Profession and Residential Address ............................................................................................:...........................................................................................
3. Age.............................................................................................................................
4. Sex ............................................................................................................................
5. Disease for which treated.......................................................................................................
6. Duration of illness........................................................................................................
7. Date of first consultation...................................................................................................... ..............................................................................................
| Date | Drug used | Form in which used | Quantity of drug used | Initials of the Regd. Medical Practitioner | Remarks |
| No. of Licence | Period of validity | ||
| (i) | Narcotic Drugs and Psychotropic Substances Act, 1985 | .................... | ............... |
| (ii) | Drugs Act, 1940 | .................... | ............... |
| Date | Opening Balance | Particulars of import certificates issued underthe Narcotic Drugs and Psychotropic Substances Act, 1985. | Particulars of licence issued if any, under thel.T.C. |
| (1) | (2) | (3) | (4) |
| Receipts | Quantity Imported | Dealer or firm from whom imported | ||
| Particulars of Export authorization issued by thecountry of origin. | Form in which the drug has been importedi.e.powder, tablet, ampules, etc. | |||
| Name | Address | |||
| (5) | (6) | (7) | (8) | (9) |
| Total Cols. 2 and 7 | Quantity issued | Purchaser's | Authority for sale (i.e.No. of Excisepermit, etc.) | |
| Name | Address | |||
| (10) | (11) | (12) | (13) | (14) |
| Mode of delivery | Closing balance | Signature of the person making the entry | Remarks |
| (15) | (16) | (17) | (18) |
| No. of Licence | Period of validity | ||
| (i) | Narcotic Drugs and Psychotropic Substances Act, 1985 | .................... | ............... |
| (ii) | Drugs Act, 1940 | .................... | ............... |
| Date | Name of Drug or preparation | Form in which purchased | Quantity |
| (1) | (2) | (3) | (4) |
| From whom received | Particulars of Licence held | Remarks | |
| Name | Address | ||
| (5) | (6) | (7) | (8) |
| Date | Name of Drug or preparation | Form in which sold | Quantity | Purchaser's | |
| Name | Address | ||||
| (1) | (2) | (3) | (4) | (5) | (6) |
| Physician's or Dentist's or Veterinary Surgeon's | Prescription Number | Particulars of licence held | Signature of person making the entry | Remarks | |
| Name | Address | ||||
| (7) | (8) | (9) | (10) | (11) | (12) |