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Agency Information Collection Activities; Submissions for Office Management and Budget Review; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application

Document ID: FDA-2011-N-0915-0002
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2012-12589
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Details Information

Document Subtype: General Notice
Received Date: May 24 2012, at 12:00 AM Eastern Daylight Time
Start-End Page: 31024 - 31025
Page Count: 2

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