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) 084644
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
USL PHARMA
Label History
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084644
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/9/1994
060
Labeling in Effect
1/23/1989
059
Labeling
3/21/1988
057
Chemistry
5/29/1986
055
Chemistry
5/29/1986
054
Chemistry
3/5/1985
052
Chemistry
3/5/1985
051
Chemistry
1/20/1982
045
Chemistry
3/30/1982
044
Chemistry
3/30/1982
043
Chemistry
5/13/1982
041
Chemistry
5/25/1982
024
Chemistry
5/25/1982
023
Chemistry
5/25/1982
022
Chemistry
2/24/1976
000
Approval
Therapeutic Equivalents
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