Guidance for industry : labeling for human prescription drug and biological products, implementing the new content and format requirements.

Bibliographic Details
Corporate Authors: Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.)
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 : Center for Biologics Evaluation and Research, [2006]
Subjects:
Online Access:https://purl.fdlp.gov/GPO/LPS118713

Internet

https://purl.fdlp.gov/GPO/LPS118713

Available Online

Holdings details from Available Online
Call Number: HE 20.4702:P 92/4/DRAFT
 
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HE 20.4702:P 92/4/DRAFT Available