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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
Description
Item Description:"Labeling."
"January 2006."
Electronic resource.
Physical Description:1 online resource (13 pages)