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Prominence of Name of Distributor of Biological Products

other · Food and Drug Administration · Rule · Published 1996-11-06 · Effective 1996-11-18 · 61 FR 57328

Document

Document number
96-28530
Federal Register citation
61 FR 57328
CFR reference
21 CFR 610
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
1996-11-06
Effective date
1996-11-18
HHS docket
Docket No. 95N-0295

Abstract

The Food and Drug Administration (FDA) is amending the labeling regulations for biological products to remove the requirement that the manufacturer's name be more prominent than that of the distributor and to permit the names of distributors to be prominently displayed on biological product container labels, package labels, and labeling. This change in labeling requirements is intended to facilitate flexible manufacturing, packaging, distribution, and labeling arrangements, and to harmonize labeling regulations applicable to biologic products licensed under the Public Health Service Act (the PHS Act) with the corresponding labeling regulations for drugs approved under the Federal Food, Drug, and Cosmetic Act (the act).

Source

Authoritative
Federal Register document
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