Exocrine Pancreatic Insufficiency Drug Products for Over-The- Counter Human Use
other · Food and Drug Administration · Rule · Published 1995-04-24 · 60 FR 20162
Document
Document number
95-10078
Federal Register citation
60 FR 20162
CFR reference
21 CFR 310
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
1995-04-24
HHS docket
Docket No. 79N-0379
Abstract
The Food and Drug Administration (FDA) is issuing a final rule establishing that over-the-counter (OTC) exocrine pancreatic insufficiency drug products (drug products used to treat pancreatic enzyme deficiency) are not generally recognized as safe and effective and are misbranded. FDA is issuing this final rule after considering public comments on the agency's notice of proposed rulemaking and all new information on OTC exocrine pancreatic insufficiency drug products that has come to the agency's attention. This final rule is part of the ongoing review of OTC drug products conducted by FDA.