Applications for Food and Drug Administration Approval To Market a New Drug; Revision of Postmarketing Reporting Requirements-Discontinuance
other · Food and Drug Administration · Rule · Published 2011-12-19 · Effective 2012-01-18 · 76 FR 78530
Document
Document number
2011-32354
Federal Register citation
76 FR 78530
CFR reference
21 CFR 314
Type
Rule
Action
Interim final rule; request for comments.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2011-12-19
Effective date
2012-01-18
HHS docket
Docket No. FDA-2011-N-0898
Abstract
The Food and Drug Administration (FDA or the Agency) is issuing an interim final rule amending its postmarketing reporting regulations implementing certain provisions of the Federal Food, Drug and Cosmetic Act. The provisions of the Federal Food, Drug and Cosmetic Act require manufacturers who are the sole manufacturers of certain drug products to notify FDA at least 6 months before discontinuance of manufacture of the products. This interim final rule modifies the term "discontinuance" and clarifies the term "sole manufacturer" with respect to notification of discontinuance requirements. The broader reporting resulting from these changes will enable FDA to improve its collection and distribution of drug shortage information to physician and patient organizations and to work with manufacturers and other stakeholders to respond to potential drug shortages.