Code of Federal Regulations, Title 21, Food and Drugs, Pt. 300-399, Revised as of April 1, 2018 (Paperback)

Code of Federal Regulations, Title 21, Food and Drugs, Pt. 300-399, Revised as of April 1, 2018 By Office of the Federal Register (U.S.) (Editor), National Archives and Records Administration (U.S.) (Editor) Cover Image

Code of Federal Regulations, Title 21, Food and Drugs, Pt. 300-399, Revised as of April 1, 2018 (Paperback)

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Special Order—Subject to Availability
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This print ISBN is the official U.S. Federal Government edition.
 

Title 21 CFR, Parts 300-499, includes updated rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and Health and Human Services (drugs for human use), investigational new drug applications, diagnostic radiopharmaceuticals, orphan drugs, bioavailability and bioequivalence requirements, over-the-counter (OTC) drug products indtended for oral ingestion that contain alcohol, OTC human drugs generally recognized as safe and effective and not misbranded, OTC digestion-related drugs, OTC antimicrobials, OTC sleep aid drugs, OTC stimulant drugs, OTC skin protectant drugs, OTC antipersperants, OTC miscellaneaous internal and external drug products, and more...

Audience: Physicians, pharmacists, medical practitioners, drug and pharmaceutical manufacturers, and the general public may be interested in this regulatory volume. 

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Product Details ISBN: 9780160945434
ISBN-10: 0160945437
Publisher: Office of the Federal Register
Publication Date: April 26th, 2018