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) 086383
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 086383
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/3/1998
035
Chemistry
8/3/1998
034
Chemistry
9/5/1997
033
Chemistry
9/5/1997
032
Chemistry
9/5/1997
031
Chemistry
3/26/1997
030
Chemistry
3/26/1997
029
Chemistry
6/22/1993
027
Labeling in Effect
8/15/1988
026
SBA
8/22/1988
025
Chemistry
8/22/1988
024
Chemistry
8/22/1988
023
Chemistry
10/5/1988
021
Chemistry
10/5/1988
020
Chemistry
6/10/1988
019
Labeling
1/17/1986
016
Chemistry
1/17/1986
015
Chemistry
1/17/1986
014
Chemistry
9/8/1978
000
Approval
Therapeutic Equivalents
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