Code of Federal Regulations, Title 21 Food and Drugs 170-199, 2023

Code of Federal Regulations, Title 21 Food and Drugs 170-199, 2023
Author: Office Of The Federal Register (U S
Publisher:
Total Pages: 0
Release: 2024-01-22
Genre: Law
ISBN: 9781636715131

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.

Code of Federal Regulations, Title 21: Parts 170-199 (Food and Drugs) FDA-Food for Human Consumption

Code of Federal Regulations, Title 21: Parts 170-199 (Food and Drugs) FDA-Food for Human Consumption
Author:
Publisher:
Total Pages:
Release: 2016-07-30
Genre:
ISBN: 9781630055547

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.

Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2022

Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2022
Author: Office Of The Federal Register (U.S.)
Publisher: Code of Federal Regulations, Title 21 Food and Drugs
Total Pages: 0
Release: 2023-05-31
Genre:
ISBN: 9781636711898

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.

Code of Federal Regulations Title 21, Food and Drugs, Parts 170-199, 2020

Code of Federal Regulations Title 21, Food and Drugs, Parts 170-199, 2020
Author: Nara
Publisher: Claitor's Pub Division
Total Pages: 652
Release: 2020-04
Genre: Law
ISBN: 9781640248007

Title 21-FOOD AND DRUGS is composed of nine volumes. The parts in these volumes are arranged in the following order: Parts 1-99, 100-169, 170-199, 200-299, 300-499, 500-599, 600-799, 800-1299 and 1300 to end. The first eight volumes, containing parts 1-1299, comprise Chapter I-Food and Drug Administration, Department of Health and Human Services. The ninth volume, containing part 1300 to end, includes Chapter II-Drug Enforcement Administration, Department of Justice, and Chapter III-Office of National Drug Control Policy.

Code of Federal Regulations, Title 21

Code of Federal Regulations, Title 21
Author: National Archives and Records Administra
Publisher:
Total Pages: 0
Release: 2010-06
Genre:
ISBN: 9781609460631

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.

Code of Federal Regulations, Title 21, Food and Drugs, PT. 500-599, Revised as of April 1, 2016

Code of Federal Regulations, Title 21, Food and Drugs, PT. 500-599, Revised as of April 1, 2016
Author: Office of the Federal Register (U S )
Publisher: Office of the Federal Register
Total Pages: 637
Release: 2016-06-21
Genre: Business & Economics
ISBN: 9780160932748

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. CFR Title 21, Parts 500-599 includes animal food labeling, common or usual names for non-standardized animal foods, new animal drugs, medicated feed mill license, food additives, substances generally recognized as safe, substances prohibited for use in animal food or feed, and more."

Code of Federal Regulations, Title 21: Parts 170-199 (Food and Drugs) FDA-Food for Human Consumption: Revised 4/08

Code of Federal Regulations, Title 21: Parts 170-199 (Food and Drugs) FDA-Food for Human Consumption: Revised 4/08
Author: National Archives and Records Administration
Publisher: U.S. Government Printing Office
Total Pages:
Release: 2008-04-01
Genre: Reference
ISBN: 9781601753311

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.

Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2020

Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2020
Author: Office Of The Federal Register (U.S.)
Publisher: Code of Federal Regulations, Title 21 Food and Drugs
Total Pages: 652
Release: 2020-11-30
Genre:
ISBN: 9781641435758

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.