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) 084678
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084678
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/3/1995
084
Labeling
11/21/1989
082
Labeling in Effect
4/7/1989
081
Labeling
1/8/1985
079
Chemistry
5/25/1984
077
Chemistry
1/13/1984
076
Chemistry
1/13/1984
075
Chemistry
6/20/1983
073
Chemistry
7/26/1982
070
Chemistry
7/26/1982
069
Chemistry
7/1/1982
068
Chemistry
3/15/1982
066
Chemistry
3/15/1982
065
Chemistry
3/15/1982
064
Chemistry
3/15/1982
062
Chemistry
3/15/1982
061
Chemistry
6/15/1976
000
Approval
Therapeutic Equivalents
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