Request for approval to publish the Import Checklist related to shelf life below 60 percent and Overprinting Snickering Stamping as per Rule 104 A of the Drugs and Cosmetics Rules 1945

By | June 26, 2026

Request for approval to publish the Import Checklist related to shelf life below 60 percent and Overprinting Snickering Stamping as per Rule 104 A of the Drugs and Cosmetics Rules 1945

 

The Gazette of India

CG-DL-E-25062026-273833

EXTRAORDINARY

PART II—Section 3—Sub-section (i)

PUBLISHED BY AUTHORITY

No. 454] NEW DELHI, MONDAY, JUNE 22, 2026/ASHADHA 1, 1948

MINISTRY OF HEALTH AND FAMILY WELFARE
(Department of Health and Family Welfare)
NOTIFICATION
New Delhi, the 22nd June, 2026

G.S.R. 505(E).— The following draft of certain rules further to amend the Drugs Rules, 1945, which the
Central Government proposes to make, in exercise of the powers conferred by sub-section (1) of section 12 and subsection (1) of section 33 of the Drugs and Cosmetics Act, 1940 (23 of 1940), after consultation with the Drugs Technical
Advisory Board is hereby published for information of all persons likely to be affected thereby, and notice is hereby
given that the said draft rules shall be taken into consideration on or after the expiry of a period of thirty days from the
date on which the copies of the Gazette of India containing these draft rules are made available to the public.
Objections and suggestions which may be received from any person within the period specified above will be
considered by the Central Government.

Objections and suggestions, if any, may be addressed to the Under Secretary Drugs), Ministry of Health and
Family Welfare, Government of India, U-6, Work Hall- C Wing, First Floor, Kartavya Bhawan-1, New Delhi, 110001
or emailed at drugsdiv-mohfw@gov.in.

(i)These rules may be called the Drugs (…… Amendment) Rules, 2026.
(ii)These rules shall come into force from the date as specified by the Government at the time of final publication of
the rules in the Official Gazette.

In the Drugs Rules, 1945, in Rule 31, the second proviso shall be substituted as follows:-
“Provided further that the licensing authority shall not allow the import of any drug having less than one year residual
shelf-life period as on the date of import. However, in the case of Biological drugs and Radiopharmaceuticals, 60% of
the labelled shelf-life may be allowed.”

[F. No. X.11014/08/2026-DR]
HARSH MANGLA, Jt. Secy.

Note: The Drugs Rules, 1945 were published in the Official Gazette vide notification No. F. 28-10/45H(1), dated the
21st December, 1945 and last amended vide notification number G.S.R.…..(E), dated the.……

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