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) 074304
Active Ingredient(s):
BETAMETHASONE DIPROPIONATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (ANDA) 074304
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/31/2002
013
Expiration Date Change
7/31/2002
012
Labeling
7/31/2002
011
Package Change
5/30/2001
010
Control Supplement
12/29/2000
009
Control Supplement
12/29/2000
008
Control Supplement
6/28/1996
007
Chemistry
6/24/1996
006
Chemistry
5/15/1996
005
Chemistry
5/15/1996
004
Chemistry
5/15/1996
003
Chemistry
5/15/1996
002
Chemistry
3/4/1996
001
Chemistry
8/31/1995
000
Approval
Therapeutic Equivalents
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