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) 070275
Active Ingredient(s):
BETAMETHASONE DIPROPIONATE
Company:
FOUGERA
Label History
Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (ANDA) 070275
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/17/1995
010
Labeling
1/6/1995
009
Chemistry
11/3/1988
008
Chemistry
11/3/1988
007
Chemistry
11/3/1988
006
Chemistry
5/29/1987
005
Chemistry
10/21/1987
004
Chemistry
3/28/1986
002
Chemistry
3/28/1986
001
Chemistry
8/12/1985
000
Approval
Therapeutic Equivalents
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