DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No:
(ANDA) 085000
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
WEST WARD
Label History
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 085000
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/21/1990
026
Chemistry
5/6/1988
025
Labeling
5/6/1988
021
Chemistry
10/3/1984
017
Chemistry
7/13/1984
016
Chemistry
11/2/1982
015
Chemistry
4/6/1977
000
Approval
Therapeutic Equivalents
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