Gazette Summary
This is NOT a Prohibition Act fee revision gazette.
Subject Matter: The Bombay Drugs (Control) Act, 1959 — Full Text
Type: Substantive Legislation (Complete Act)
Nature of Document
This gazette presents the complete enacted text of the Bombay Drugs (Control) Act, 1959 (Bombay Act No. XI of 1960), including all amendments through Maharashtra Act No. 52 of 1973. It is not a fee revision notification or a rule amendment gazette under the Bombay Prohibition Act, 1949 (BPA).
Scope and Authority
Statutory Authority: The Act was enacted under the Republic of India's legislative powers in the Tenth year of the Republic (1960), received Presidential assent on 4th February 1960, and was published in the Maharashtra Government Gazette on 9th February 1960.
Territorial Extent: The entire State of Maharashtra.
Commencement: 1st January 1962 (vide G.N., H.D., No. BDC.1059/37596-III, dated 18th November 1961).
Subsequent Amendments:
- Maharashtra Act 51 of 1971
- Maharashtra Act 52 of 1973 (effective 14-1-1974)
- Modified by the Maharashtra Adaptation of Laws (State and Concurrent Subjects) Order, 1960
Legislative Purpose
Objective: To provide for the control, in the interests of the general public, of the:
- Sale
- Possession
- Transport
- Use of certain drugs (medicines and substances intended for human or animal treatment)
The Act aims to prevent misuse of drugs injurious to health while regulating legitimate medical and commercial use.
Key Regulatory Framework
1. Administration (Sections 3-5)
- Commissioner of Prohibition and Excise: Appointed under BPA 1949, exercises superintendence and powers conferred by this Act, subject to State Government control.
- Collectors: Exercise jurisdiction within their districts; State Government may appoint other officers to perform Collector's functions.
- Hierarchical Control: All officers are subordinate to the Commissioner and State Government.
2. Notified Drugs (Section 6)
- State Government may, by notification in the Official Gazette, declare any drug to be subject to this Act.
- If a drug is used in a manner injurious to health, it may be specifically notified as a "notified drug" — triggering stringent licensing and possession controls.
3. Licensing Requirements (Section 7)
- Mandatory Licence: From a date fixed by notification, no person may carry on business as a wholesaler or retailer in any notified drug except under a licence granted by the Collector.
- Licence forms, terms, conditions, and fees are prescribed by rules.
4. Sale Restrictions (Sections 8-11)
- Retailers: May only procure notified drugs from licensed wholesalers (Section 8).
- Dealers (wholesalers/retailers): May sell to medical practitioners or persons authorised under Section 14 (Section 9).
- Maximum Quantities: State Government may fix maximum quantities sold in any one transaction (Section 10) — different maxima for different drugs, classes of sellers, and buyers.
- Prescription Requirement (Section 11):
- Licensed retailers and medical practitioners must supply notified drugs only for bona fide medicinal purposes and only on prescription issued by a medical practitioner.
- Prescriptions and records must be maintained and preserved as prescribed.
5. Possession Limits (Section 12)
- Dealers/Medical Practitioners: May possess notified drugs up to prescribed quantities; medical practitioners require Collector's written permission for excess quantities.
- General Public: May possess only quantities dispensed or sold on prescription for bona fide medicinal use of self or household members, except under permit granted by empowered officer.
- Exception: Travellers entering the State from outside with notified drugs for medicinal use of self or household are exempt.
6. Transport Restrictions (Section 13)
- Dealers: Must obtain a pass from an empowered officer to transport notified drugs.
- Medical Practitioners/Others: May transport only quantities they are permitted to possess; excess requires a pass.
- Exemptions: Travellers entering the State; through-transport from one place outside the State to another outside.
7. Special Authorisations (Section 14)
- Collector may, by general or special order, authorise:
- Hospitals/dispensaries (for medical use)
- Educational institutions (for educational purposes)
- Scientific researchers (for research)
- Aircraft pilots (emergency use)
- Ambulances/first-aid stations (emergency use)
- Chemists (as ingredient in medicines)
- Manufacturers (for manufacturing)