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) 089109
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for PROMETHAZINE HYDROCHLORIDE, (ANDA) 089109
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/30/2001
003
Facility Addition
2/18/1988
002
Chemistry
9/10/1985
000
Approval
Therapeutic Equivalents
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