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Guidance for industry : dosage and administration 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, [2007]
Subjects:
Drugs > Labeling.
Drugs > Dosage.
Biologicals > Labeling.
Online Access:https://purl.fdlp.gov/GPO/LPS118599
Description
Item Description:"Draft guidance."
"Labeling."
"April 2007."
Electronic resource.
Physical Description:1 online resource (i, 10 pages)