DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MOEXIPRIL HYDROCHLORIDE
FDA Application No:
(ANDA) 077536
Active Ingredient(s):
MOEXIPRIL HYDROCHLORIDE
Company:
PADDOCK
Label History
Labels are not available on this site for MOEXIPRIL HYDROCHLORIDE, (ANDA) 077536
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/30/2006
000
Approval
Other Important Information from FDA
Therapeutic Equivalents
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