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)

21:4.0.1.1	SUBCHAP C	SUBCHAPTER C - DRUGS: GENERAL
21:4.0.1.1.1	PART 200	PART 200 - GENERAL
21:4.0.1.1.2	PART 201	PART 201 - LABELING
21:4.0.1.1.3	PART 202	PART 202 - PRESCRIPTION DRUG ADVERTISING
21:4.0.1.1.4	PART 203	PART 203 - PRESCRIPTION DRUG MARKETING
21:4.0.1.1.5	PART 205	PART 205 - GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
21:4.0.1.1.6	PART 206	PART 206 - IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
21:4.0.1.1.7	PART 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
21:4.0.1.1.8	PART 208	PART 208 - MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
21:4.0.1.1.9	PART 209	PART 209 - REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
21:4.0.1.1.10	PART 210	PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
21:4.0.1.1.11	PART 211	PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
21:4.0.1.1.12	PART 212	PART 212 - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
21:4.0.1.1.13	PART 216	PART 216 - HUMAN DRUG COMPOUNDING
21:4.0.1.1.14	PART 225	PART 225 - CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
21:4.0.1.1.15	PART 226	PART 226 - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
21:4.0.1.1.16	PART 250	PART 250 - SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
21:4.0.1.1.17	PART 251	PART 251 - SECTION 804 IMPORTATION PROGRAM
21:4.0.1.1.18	PART 290	PART 290 - CONTROLLED DRUGS
21:4.0.1.1.19	PART 299	PART 299 - DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES

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