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Code of Federal Regulations Title 21, Volume 5, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 5, April 1, 2017 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 300 to 499, Food and Drugs This volume contains Parts 300 to 499: - Part 300; GENERAL - Part 310; NEW DRUGS - Part 312; INVESTIGATIONAL NEW DRUG APPLICATION - Part 314; APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG - Part 315; DIAGNOSTIC RADIOPHARMACEUTICALS - Part 316; ORPHAN DRUGS - Part 317; QUALIFYING PATHOGENS - Part 320; BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS - Part 328; OVER-THE-COUNTER DRUG PRODUCTS INTENDED FOR ORAL INGESTION THAT CONTAIN ALCOHOL - Part 329; NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT - Part 330; OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED - Part 331; ANTACID PRODUCTS FOR OVER-THE-COUNTER (OTC) HUMAN USE - Part 332; ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 333; TOPICAL ANTIMICROBIAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 335; ANTIDIARRHEAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 336; ANTIEMETIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 338; NIGHTTIME SLEEP-AID DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 340; STIMULANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 341; COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 343; INTERNAL ANALGESIC, ANTIPYRETIC, AND ANTIRHEU-MATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 344; TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 346; ANORECTAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE - Part 347; SKIN PROTECTANT DRUG PRODUCTS FOR OVER-T
This volume codifies the federal regulations governing food and drugs in the United States. It specifically details Parts 300 through 499 of Title 21 of the Code of Federal Regulations as of April 1, 2017. The content covers a broad spectrum of regulatory requirements, including general provisions, new drug applications, bioavailability, and over-the-counter drug products.
This compilation serves as a critical reference for legal professionals, pharmaceutical companies, researchers, and regulatory bodies involved with food and drug administration in the United States. Its value lies in providing direct access to the codified regulations that dictate the approval, marketing, and safety standards for these products. The specific date of April 1, 2017, indicates its utility as a snapshot of the regulatory landscape at that particular time, essential for historical accuracy and compliance checks.
Page Count:
402
Publication Date:
2017-09-19
Publisher:
Creative Media Partners, LLC
ISBN-10:
1298709032
ISBN-13:
9781298709035
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