# Distribution of Certain Drug Products by Registered Blood Establishments and Comprehensive Hemophilia Diagnostic Treatment Centers That Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements and Administrative Procedures
> **Food and Drug Administration** · Final rule. · Published 2008-10-09 · Effective 2008-11-10 · 73 FR 59496
## Document
- **Document number:** E8-24050
- **Category:** hospital-facility
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 73 FR 59496
- **CFR reference:** 21 CFR 203
- **Publication date:** 2008-10-09
- **Effective date:** 2008-11-10
- **HHS docket:** Docket No. FDA-2005-N-0345
## Abstract

The Food and Drug Administration (FDA) is amending its regulations to allow certain registered blood establishments and comprehensive hemophilia diagnostic treatment centers that are also health care entities to distribute certain drug products. The final rule amends limited provisions of the regulations implementing the Prescription Drug Marketing Act of 1987 (PDMA), as modified by the Prescription Drug Amendments of 1992 (PDA). These regulations, among other things, restrict the sale, purchase, or trade of, or the offer to sell, purchase, or trade, prescription drugs purchased by hospitals and other health care entities.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2008/10/09/E8-24050/distribution-of-certain-drug-products-by-registered-blood-establishments-and-comprehensive)
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