DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BEPADIN
FDA Application No:
(NDA) 019001
Active Ingredient(s):
BEPRIDIL HYDROCHLORIDE
Company:
MEDPOINTE PHARM HLC
Label History
Labels are not available on this site for BEPADIN, (NDA) 019001
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/28/1990
000
Approval
Therapeutic Equivalents
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