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FEDERAL REGISTER · PROPOSED RULEMarch 20, 2024PROPOSED — NOT IN FORCE

Drug Products or Categories of Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A or 503B of the Federal Food, Drug, and Cosmetic Act

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Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.

STATUSPROPOSED — NOT IN FORCE
PROPOSED EFFECTIVE—
COMMENTS CLOSEJun 18, 2024 · closed
APPLIES TO · SPEQ TAGDrug
Document type
Proposed Rule
Agency
Health and Human Services Department
Published
March 20, 2024
Comments close
June 18, 2024
Document number
2024-05801
CFR references
21 CFR 216
Docket
FDA-2023-N-0061
RIN
0910-AI31
ABSTRACT

The Food and Drug Administration is proposing to establish criteria for the lists of drug products or categories of drug products that present demonstrable difficulties for compounding (Demonstrable Difficulties for Compounding Lists or DDC Lists) under certain sections of the Federal Food, Drug, and Cosmetic Act. Additionally, the Agency is proposing to identify the first three categories of drug products on both DDC Lists. Drug products or categories of drug products that appear on the DDC Lists cannot qualify for certain statutory exemptions, and therefore may not be compounded under, either section 503A or section 503B, respectively.

Abstract as published in the Federal Register.

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