DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIAZEPAM
FDA Application No:
(ANDA) 071310
Active Ingredient(s):
DIAZEPAM
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for DIAZEPAM, (ANDA) 071310
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/25/1994
005
Labeling
6/16/1993
004
Chemistry in Effect
1/18/1991
003
Labeling
1/21/1988
001
Chemistry
7/17/1987
000
Approval
Therapeutic Equivalents
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