DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BETAMETHASONE DIPROPIONATE
FDA Application No:
(ANDA) 072538
Active Ingredient(s):
BETAMETHASONE DIPROPIONATE
Company:
PERRIGO NEW YORK
Label History
Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (ANDA) 072538
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/1997
005
Labeling
1/24/1997
004
Labeling
5/5/1995
003
Chemistry
1/31/1990
000
Approval
Therapeutic Equivalents
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