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Electronic Code of Federal Regulations

e-CFR data is current as of July 8, 2020

Title 21Chapter ISubchapter CPart 203


TITLE 21—Food and Drugs

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

SUBCHAPTER C—DRUGS: GENERAL

PART 203—PRESCRIPTION DRUG MARKETING

rule

Subpart A—GENERAL PROVISIONS

§203.1
Scope.
§203.2
Purpose.
§203.3
Definitions.
rule

Subpart B—REIMPORTATION

§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.
rule

Subpart C—SALES RESTRICTIONS

§203.20
Sales restrictions.
§203.22
Exclusions.
§203.23
Returns.
rule

Subpart D—SAMPLES

§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.
rule

Subpart E—WHOLESALE DISTRIBUTION

§203.50
Requirements for wholesale distribution of prescription drugs.
rule

Subpart F—REQUEST AND RECEIPT FORMS, REPORTS, AND RECORDS

§203.60
Request and receipt forms, reports, and records.
rule

Subpart G—REWARDS

§203.70
Application for a reward.

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