Last Updated on June 25, 2026 by The Health Master

Schedules: for Drugs

 

Schedules – for drugs under Drugs and Cosmetics Act 1940 and Rules 1945

 

 

Rules Law
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As per the Drugs and Cosmetics Act 1940 and Rules 1945, we have provided some important schedules for drugs relevant to the above-mentioned topic. Click the below links for more information:

 

Schedule-B

Schedule-B: Fees for test or analysis by the Central Drugs Laboratories or State Drugs Laboratories

 

 

Schedule-C, C1

Schedule-C-C1: Biological and special products

 

 

Schedule-D

Schedule-D: Class of drugs and Extent and conditions of exemption

 

 

Schedule-D I

Schedule-D1: Information and undertaking required to be submitted by the manufacturer or his authorized agent with the Application Form for a Registration Certificate

 

 

Schedule-D II

Schedule-DII: Information required to be submitted by the manufacturer or his authorized agent with the Application Form for the Registration of a Bulk Drug/Formulation/ Product for its import into India

 

 

Schedule-F

Requirements for the functioning and operation of a blood bank and / or for preparation of blood components

 

 

Schedule-F I

Provisions applicable to the production of bacterial vaccines

 

 

Schedule-F II

Standards for surgical dressings

 

 

Schedule-F III

Standards for umbilical tapes

 

 

Schedule-FF

Standards for ophthalmic preparations

 

 

Schedule-G

Schedule-G: List of drugs falls under Schedule-G

 

 

Schedule-H

Schedule-H: List of drugs falls under Schedule-H

 

 

Schedule-H 1

Schedule-H1: List of drugs falls under Schedule H1

 

 

Schedule-H 2

Schedule-H2: List of 300 drugs falls under Schedule H2 for printing Bar Code or QR Code

Schedule-H2

GSR 506(E) dt 22-06-2026 Notification regarding Schedule H2 drugs insertion of Table 1 and Table 2 regarding Vaccines, Antimicrobials, NDPS and Anticancer drugs

GSR 506(E) dt 22-06-2026 Notification regarding Schedule H2 drugs insertion of Table 1 and Table 2 regarding Vaccines, Antimicrobials, NDPS and Anticancer drugs

 

Schedule-J

Diseases and ailments (by whatever name described) which a drug may not purport to prevent or cure or make claims to prevent or cure.

 

 

Schedule-K

Schedule-K: Class of drugs and Extent and Conditions of Exemption

 

 

Schedule-L 1

Schedule-L1: (GLP) Good laboratory practices and requirements of premises and equipment

 

 

Schedule-M

Schedule-M: (GMP) Good manufacturing practices for premises and materials

 

Revised Schedule M

 

Schedule-M I

Good manufacturing practices and requirements of premises, plant and equipment for homoeopathic medicines

 

 

Schedule-N

List of minimum equipment for the efficient running of a pharmacy

 

 

Schedule-O

Schedule-O: Provisions applicable to Black Fluids and White Fluids

 

 

Schedule-P

Schedule-P: Storage conditions of drugs

 

 

Schedule-P 1

Schedule-P1: Pack size of drugs

 

 

Schedule-Q

List of dyes, colours and pigments permitted to be used in cosmetics and soaps as given under is : 4707

 

 

Schedule-R

Standards for condoms made of rubber latex intended for single use and other mechanical contraceptives

 

 

Schedule-R I

The medical devices shall conform to the Indian Standards laid down from time to time by the Bureau of Indian Standards. If there are no Bureau of Indian Standards then it shall conform to the International Standards, like International Organisation for Standardisation, or other International Pharmacopeia Standards and such other standards as may be specified for this purpose. In case national or international standards are not available, the device shall conform to the manufacturer‘s validated standards.

 

 

Schedule-S

Standards for cosmetics

 

 

Schedule-T

Schedule-T: (GMP) Good manufacturing practices for Ayurvedic, Siddha and Unani medicines

 

 

Schedule-T A

Schedule-T-A: Form for record of utilizaion of raw material by Ayurveda or Siddha or Unani licensed manufacturing units during the financial year

 

 

Schedule-U

Particulars to be shown in manufacturing records

 

 

Schedule-U I

Particulars to be shown in the manufacturing records

 

 

Schedule-V

Standards for patent or proprietary medicines

 

 

Schedule-X

Schedule-X: List of drugs falls under Schedule-X

 

 

Schedule-Y

Schedule-Y: Requirements and guidelines for permission to import and / or manufacture of new drugs for sale or to undertake clinical trials

 

 

Schedules: All types of Drugs

Schedules: All types of Cosmetics

Schedules: All types of Medical Devices

Schedules: All types of Clinical Trials

 

Forms: Drugs

Forms: Cosmetics

Forms: Medical Devices

Forms: Clinical Trial

 

 

 

 

Licensing procedure for manufacturing of Drugs

 

Latest Notifications: D&C Rules 1945

 

Latest Notifications: D&C Act 1940