Part 203 — Prescription Drug Marketing
Current through Sep 8, 2026
Authority: 21 U.S.C. 331, 333, 351, 352, 353, 360, 371, 374, 381.
Source: 64 FR 67756, Dec. 3, 1999, unless otherwise noted.
Sections
- § 203.1 Scope.
- § 203.2 Purpose.
- § 203.3 Definitions.
- § 203.10 Restrictions on reimportation.
- § 203.11 Applications for reimportation to provide emergency medical care.
- § 203.12 An appeal from an adverse decision by the district office.
- § 203.20 Sales restrictions.
- § 203.22 Exclusions.
- § 203.23 Returns.
- § 203.30 Sample distribution by mail or common carrier.
- § 203.31 Sample distribution by means other than mail or common carrier (direct delivery by a representative or detailer).
- § 203.32 Drug sample storage and handling requirements.
- § 203.33 Drug sample forms.
- § 203.34 Policies and procedures; administrative systems.
- § 203.35 Standing requests.
- § 203.36 Fulfillment houses, shipping and mailing services, comarketing agreements, and third-party recordkeeping.
- § 203.37 Investigation and notification requirements.
- § 203.38 Sample lot or control numbers; labeling of sample units.
- § 203.39 Donation of drug samples to charitable institutions.
- § 203.50 Requirements for wholesale distribution of prescription drugs.
- § 203.60 Request and receipt forms, reports, and records.
- § 203.70 Application for a reward.