Food and Drugs Administration, (FDA) Haryana, India. |
Email ID: dahiya19@yahoo.com
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Last Updated on November 28, 2023 by The Health Master
Schedules –All types of Drugs under Drugs and Cosmetics Act 1940 and Rules 1945
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 on 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-B
Schedule-C, C1
Schedule-C-C1: Biological and special products
Schedule-C-C1
Schedule-D
Schedule-D: Class of drugs and Extent and conditions of exemption
Schedule-D
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-D1
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 / special product for its import into India
Schedule-D-II
Schedule-F I
Provisions applicable to the production of bacterial vaccines
Schedule-F-I
Schedule-F II
Standards for surgical dressings
Schedule-F-II
Schedule-F III
Standards for umbilical tapes
Schedule-F-III
Schedule-FF
Standards for ophthalmic preparations
Schedule-FF
Schedule-G
Schedule-G: List of drugs falls under Schedule-G
Schedule-G
Schedule-H
Schedule-H: List of drugs falls under Schedule-H
Schedule-H
Schedule-H1
Schedule-H1: List of drugs falls under Schedule H1
Schedule-H1
Schedule-H 2
Schedule-H2: List of 300 drugs falls under Schedule H2 for printing Bar Code or QR Code
Schedule-H2
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-J
Schedule-K
Schedule-K: Class of drugs and Extent and Conditions of Exemption
Schedule-K
Schedule-L1
Schedule-L1: (GLP) Good laboratory practices and requirements of premises and equipment
Schedule-L1
Schedule-M
Schedule-M: (GMP) Good manufacturing practices for premises and materials
Schedule-M
Schedule-M I
Good manufacturing practices and requirements of premises, plants and equipment for homeopathic medicines
Schedule-M-I
Schedule-N
List of minimum equipment for the efficient running of a pharmacy
Schedule-N
Schedule-O
Schedule-O: Provisions applicable to Black Fluids and White Fluids
Schedule-O
Schedule-P
Schedule-P: Storage conditions of drugs
Schedule-P
Schedule-P1
Schedule-P1: Pack size of drugs
Schedule-P1
Schedule-Q
List of dyes, colors and pigments permitted to be used in cosmetics and soaps as given under is : 4707
Schedule-Q
Schedule-R
Standards for condoms made of rubber latex intended for single use and other mechanical contraceptives
Schedule-R
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 is no Bureau of Indian Standards, then it shall conform to the international standards like those of the International Organization for Standardization, 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-R-I
Schedule-S
Standards for cosmetics
Schedule-S
Schedule-T
Schedule-T: (GMP) Good manufacturing practices for Ayurvedic, Siddha and Unani medicines
Schedule-T
Schedule-TA
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-T-A
Schedule-U
Particulars to be shown in manufacturing records
Schedule-U
Schedule-U I
Particulars are to be shown in the manufacturing records
Schedule-U-I
Schedule-V
Standards for patent or proprietary medicines
Schedule-V
Schedule-X
Schedule-X: List of drugs falls under Schedule-X
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
Schedule-Y
Compiled by:
Rakesh Dahiya, SDCO cum Licensing Authority, FDA Haryana
Licensing procedure for manufacturing of Drugs
Latest Notifications: D&C Rules 1945
Latest Notifications: D&C Act 1940
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