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GUIDANCE DOCUMENT

Withdrawn CDER Product Specific Guidances September 2021

Final
Docket Number:
FDA-2007-D-0369
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

Updated September 9, 2021


Submit Comments

You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2007-D-0369.

 
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