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) 084887
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
MYLAN
Label History
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084887
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/10/1981
058
Chemistry
6/10/1981
057
Chemistry
6/10/1981
056
Chemistry
6/10/1981
055
Chemistry
Therapeutic Equivalents
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