Title 21

Volume 4 CHAPTER I

Chapter I - Food And Drug Administration, Department Of Health And Human Services (continued)

CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

21:4.0.1.1SUBCHAP C
SUBCHAPTER C - DRUGS: GENERAL
21:4.0.1.1.1PART 200
   PART 200 - GENERAL
21:4.0.1.1.2PART 201
   PART 201 - LABELING
21:4.0.1.1.3PART 202
   PART 202 - PRESCRIPTION DRUG ADVERTISING
21:4.0.1.1.4PART 203
   PART 203 - PRESCRIPTION DRUG MARKETING
21:4.0.1.1.5PART 205
   PART 205 - GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
21:4.0.1.1.6PART 206
   PART 206 - IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
21:4.0.1.1.7PART 207
   PART 207 - 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
21:4.0.1.1.8PART 208
   PART 208 - MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
21:4.0.1.1.9PART 209
   PART 209 - REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
21:4.0.1.1.10PART 210
   PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
21:4.0.1.1.11PART 211
   PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
21:4.0.1.1.12PART 212
   PART 212 - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
21:4.0.1.1.13PART 216
   PART 216 - HUMAN DRUG COMPOUNDING
21:4.0.1.1.14PART 225
   PART 225 - CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
21:4.0.1.1.15PART 226
   PART 226 - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
21:4.0.1.1.16PART 250
   PART 250 - SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
21:4.0.1.1.17PART 290
   PART 290 - CONTROLLED DRUGS
21:4.0.1.1.18PART 299
   PART 299 - DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES