Guidance for industry : adverse reactions section of labeling for human prescription drug and biological products, content and format.

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:	Drugs > Side effects > United States. Drugs > Labeling > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS118495

Available Online