Cfr Title 21 Pt 200-299 ; Code Of Federal Regulations(2021)

Cfr Title 21 Pt 200-299 ; Code Of Federal Regulations(2021)
Title:
Code of Federal Regulations, Title 21, Food and Drugs, Pt 200-299, Revised as of April 1, 2021
Agency Publisher: 
National Archives and Records Administration (NARA)
Office of the Federal Register (OFR)
Format:
Paperback
USA Price: 
$39.00 Display Foreign Price
Stock:
Preorder
GPO Stock Number:
869-094-00071-4
ISBN:
9780160961052
Description

21 CFR, Pts. 200-299, includes rules, regulations, procedures and administrative procedures associated with TITLE 21—Food and Drugs, CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED), SUBCHAPTER C—DRUGS: GENERAL.

Table of Contents

 

200

200.5 to 200.200

GENERAL

201

201.1 to 201.328

LABELING

202

202.1

PRESCRIPTION DRUG ADVERTISING

203

203.1 to 203.70

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

207.1 to 207.81

REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE

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

HUMAN DRUG 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

251

251.1 to 251.21

SECTION 804 IMPORTATION PROGRAM

290

290.1 to 290.10

CONTROLLED DRUGS

299

299.3 to 299.5

DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES

Audience

Lawyers, law librarians and law students should be familiar with the Code of Federal Regulations. Law libraries and some academic libraries should have a copy of this publication for their patrons. In addition, members of government and policymakers, members of Congress, tax preparers, investment counselors and brokers, social activists, political consultants, media writers and producers, university instructors and professors, political scientists, and taxpayers.                                                                                                   

Product Details

Availability Details:
Available for Pre-order
USA Price:
$39.00
International Price:
$54.60
Publisher:
National Archives and Records Administration, Office of the Federal Register
Key Phrases:
  • CFR Title 21
  • Food and Drugs
Quantity Price:
Discount
Cover:
Paper
Unit of Issue (US):
1
Unit of Issue (Non-US):
1
Record Creation Date:
05/12/2021
Last Status Update:
06/08/2021
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