Cfr Title 21 Pt 200-299 ; Code Of Federal Regulations(paper)2019

Cfr Title 21 Pt 200-299       ; Code Of Federal Regulations(paper)2019
Title:
Code of Federal Regulations, Title 21, Food and Drugs, Part 200-299, Revised as of April 1, 2019
Format:
Paperback
USA Price: 
Stock:
In stock
GPO Stock Number:
869-090-00070-1
ISBN:
9780160951787
Description

In this official 21CFR Parts 200-299, you will find updated rules, procedures, regulations, and processes relating to the U.S. Department of Health and Human Services, especially within the Food and Drug Administration.

 

  • This edition focuses on these key areas:
  • Drug packaging and labeling,
  • Manufacturing of drugs and guidelines,
  • Controlled drugs, 
  • Medication Guides for Prescription Drugs
  • and more
  •  

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FDA Drug Folders

 

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

290

290.1 to 290.10

CONTROLLED DRUGS

299

299.3 to 299.5

DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES

Description

Drug manufacturers, health advocates and policy makers, drug packagers, physicians, nurse practitioners, pharmacuetical staff, pharmacy staff, and health practice attorneys may be interested in this offiical regulatory volume.   Students pursuing coursework for M.D. and speciality medical degree programs may also be interesteted in this volume, along with laboratory scientists within the medical field. 

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
Key Phrases:
  • CFR Title 21
Weight:
0.75
Quantity Price:
Discount
Cover:
Paper
Unit of Issue (US):
1
Unit of Issue (Non-US):
1
Record Creation Date:
06/13/2019
Last Status Update:
08/05/2020
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