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Code of Federal Regulations, Title 21, Food and Drugs, Pt. 200-299, Revised as of April 1, 2017

Title:
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 200-299, Revised as of April 1, 2017
Format:
Paperback
USA Price: 
Stock:
In stock
GPO Stock Number:
869-086-00071-1
ISBN:
9780160938122
Description

Title 21 CFR, Parts 200-299, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and Department of Health and Human Services (drugs), labeling, prescription drug advertising and marketing, guidelines for state licensing of wholesale prescription drug distributors, medication guides for prescription drugs, requirement for authorized dispensers and pharmacies to distribute a side effects statement, special requirements for specific human drugs, controlled drugs, and more...

 

EST. DELIVERY DATE 07/25/17.

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Table of Contents

Table of Contents:
Title 21 → Chapter I → Subchapter C
TITLE 21—Food and Drugs
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
SUBCHAPTER C—DRUGS: GENERAL
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 216.24
CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
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

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, as well as Members of Congress would find this publication useful.

Physicians; hospital personnel, including administrators and nurse practitioners; drug/pharmaceutical manufacturers; drug marketers and advertisers; pharmacists; and public citizens may be interested in this volume.  

Product Details

Availability Details:
In Stock
USA Price:
$20.00
International Price:
$28.00
Publisher:
National Archives and Records Administration, Office of the Federal Register
Year/Pages:
2017: 256 p.
Key Phrases:
  • CFR Title 21
Weight:
0.6875
Quantity Price:
Discount
Cover:
Paper
Unit of Issue (US):
1
Unit of Issue (Non-US):
1
Item available Date:
04/25/2017
Last Status Update:
10/18/2017
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