DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FINASTERIDE
FDA Application No:
(ANDA) 077251
Active Ingredient(s):
FINASTERIDE
Company:
GEDEON RICHTER USA
Label History
Labels are not available on this site for FINASTERIDE, (ANDA) 077251
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/27/2006
000
Tentative Approval
12/26/2006
000
Approval
Therapeutic Equivalents
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