Code of Federal Regulations, Title 21, Food and Drugs, Pt. 200-299, Revisedas of

Code of Federal Regulations, Title 21, Food and Drugs, Pt. 200-299, Revised as of April 1, 2016

Agency Publisher: National Archives and Records Administration, Office of the Federal Register
USA List Price:
$20.00 Display International Price
Availability:
In Stock
GPO Stock Number: 869-084-00070-1 ISBN: 9780160932724
Price: $20.00

Description

CFR Title 21, Parts 200-299 include labeling, prescription drug advertising, prescription drug marketing, registration of producers of drugs and listing of drugs in commercial distribution, medication guides to prescription drugs, pharmacy compounding, controlled drugs, official drug names and established drug names, and more.

Table of Contents:
200
200.5 to 200.200 GENERAL
201
201.1 to 201.327 LABELING
202
202.1 PRESCRIPTION DRUG ADVERTISING
203
PRESCRIPTION DRUG MARKETING
205
205.1 to 205.50 GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
206
206.1 to 206.10 IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
207
207.3 to 207.40 REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION
208
208.1 to 208.26 MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
209
209.1 to 209.11 REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
210
210.1 to 210.3 CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
211
211.1 to 211.208 CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
212
212.1 to 212.110 CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
216
216.23 to 216.24 PHARMACY COMPOUNDING
225
225.1 to 225.202 CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
226 226.1 to 226.115 CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
250
250.11 to 250.250 SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
290
290.1 to 290.10 CONTROLLED DRUGS
299
299.3 to 299.5 DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES

Audience: Target audience are drug marketers and advertisers, pharmacists, and public citizens interested in regulations for prescription drugs and pharmaceuticals.

Keywords: 21cfr, 21CFR, CFR 21, CFR title 21 parts 200-299, Code of Federal Regulations food and drugs, CFR title 21 April 1 2016, food and drug regulations, pharmaceutical regulations, prescription drug laws, prescription drug dosage laws, registration of commercial drugs, cfr 21 2016 food and drugs pt 200-299

Product Details

GPO Stock Number:
869-084-00070-1
ISBN:
9780160932724
Availability Details:
In Stock - Warehouse and Retail (Priced)
USA Price:
$20.00
International Price:
$28.00
Publisher:
National Archives and Records Administration, Office of the Federal Register
Author:
 
Year/Pages:
2016: 249 p.
Note:
 
Key Phrases:
CFR Title 21
SuDocs Class:
 
Weight:
0.75 lb.
Quantity Price:
Discount
Binding:
Paperback
Cover:
Paper
Subject Bibliography:
 
Unit of Issue (U.S.):
Each
Item Available Date:
07/15/2016
Last Status Update:
04/28/2017