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

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Format:
Book
Government document
Contributor:
Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Language:
English
Subjects (All):
Drugs--Labeling.
Drugs.
Biologicals--Labeling.
Biologicals.
Biological products--Labeling.
Biological products.
Physical Description:
1 online resource (27 pages)
Other Title:
Labeling for human prescription drug and biological products, implementing the new content and format requirements
Place of Publication:
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]
Notes:
"Draft guidance."
"Labeling."
"January 2006."
OCLC:
499109706

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