DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HALOBETASOL PROPIONATE
FDA Application No:
(ANDA) 077109
Active Ingredient(s):
HALOBETASOL PROPIONATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for HALOBETASOL PROPIONATE, (ANDA) 077109
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/14/2005
000
Approval
Therapeutic Equivalents
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