21 CFR Part 203 - PRESCRIPTION DRUG MARKETING
- Subpart A - General Provisions (§§ 203.1 - 203.3)
- Subpart B - Reimportation (§§ 203.10 - 203.12)
- Subpart C - Sales Restrictions (§§ 203.20 - 203.23)
- Subpart D - Samples (§§ 203.30 - 203.39)
- Subpart E - Wholesale Distribution (§ 203.50)
- Subpart F - Request and Receipt Forms, Reports, and Records (§ 203.60)
- Subpart G - Rewards (§ 203.70)
{'United States Code': [{'Title': '21', 'Section': '331', 'headtext': ' Prohibited acts', 'cleanpath': '/uscode/text/21/331'}, {'Title': '21', 'Section': '333', 'headtext': ' Penalties', 'cleanpath': '/uscode/text/21/333'}, {'Title': '21', 'Section': '351', 'headtext': ' Adulterated drugs and devices', 'cleanpath': '/uscode/text/21/351'}, {'Title': '21', 'Section': '352', 'headtext': ' Misbranded drugs and devices', 'cleanpath': '/uscode/text/21/352'}, {'Title': '21', 'Section': '353', 'headtext': ' Exemptions and consideration for certain drugs, devices, and biological products', 'cleanpath': '/uscode/text/21/353'}, {'Title': '21', 'Section': '360', 'headtext': ' Registration of producers of drugs or devices', 'cleanpath': '/uscode/text/21/360'}, {'Title': '21', 'Section': '371', 'headtext': ' Regulations and hearings', 'cleanpath': '/uscode/text/21/371'}, {'Title': '21', 'Section': '374', 'headtext': ' Inspection', 'cleanpath': '/uscode/text/21/374'}, {'Title': '21', 'Section': '381', 'headtext': ' Imports and exports', 'cleanpath': '/uscode/text/21/381'}], 'Statutes at Large': [], 'Public Laws': [], 'Presidential Documents': []}