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) 071882
Active Ingredient(s):
BETAMETHASONE DIPROPIONATE
Company:
TEVA PHARMS
Label History
Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (ANDA) 071882
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/17/1999
006
Chemistry
3/23/1999
005
Chemistry
6/11/1998
004
Chemistry
5/31/1996
003
Chemistry
8/18/1992
002
Labeling
7/10/1992
001
Chemistry
6/6/1988
000
Approval
Therapeutic Equivalents
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