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:
(NDA) 019141
Active Ingredient(s):
BETAMETHASONE DIPROPIONATE
Company:
FOUGERA
Label History
Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (NDA) 019141
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/7/1996
014
Chemistry
8/17/1995
013
Labeling
6/7/1996
012
Chemistry
7/16/1992
011
Chemistry in Effect
11/1/1988
010
Chemistry
11/1/1988
009
Chemistry
11/1/1988
008
Chemistry
4/23/1987
007
Chemistry
7/6/1987
006
Chemistry
10/20/1987
005
Chemistry
6/27/1986
002
Chemistry
3/28/1986
001
Chemistry
9/4/1984
000
Approval
Therapeutic Equivalents
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