DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROMETHAZINE HYDROCHLORIDE
FDA Application No:
(ANDA) 084555
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for PROMETHAZINE HYDROCHLORIDE, (ANDA) 084555
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
016
Chemistry
12/23/1994
015
Chemistry
10/11/1994
014
Chemistry
4/3/1992
013
Chemistry
4/3/1992
011
Chemistry
4/10/1987
010
Chemistry
7/29/1976
000
Approval
Therapeutic Equivalents
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