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GUIDANCE DOCUMENT

ANDAs: Impurities in Drug Products Guidance for Industry November 2010

Download the Final Guidance Document Read the Federal Register Notice
Final
Docket Number:
FDA-2010-D-0584
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

This guidance provides recommendations on what chemistry, manufacturing, and controls (CMC) information sponsors should include regarding the reporting, identification, and qualification of impurities that are classified as degradation products in drug products when submitting.

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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:

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5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2010-D-0584.

 
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