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Guidance for industry : ANDAs, impurities in drug products.

Bibliographic Details
Corporate Authors: Center for Drug Evaluation and Research (U.S.), Center for Drug Evaluation and Research (U.S.). Office of Generic Drugs
Format: Government Document eBook
Language:English
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2005]
Subjects:
Drug adulteration > Government policy > United States.
Drug approval > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS117044
Description
Item Description:"OGD."
"Revision 1."
"August 2005."
Electronic resource.
Physical Description:1 online resource (8 pages) : chart.