DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CLOBETASOL PROPIONATE
FDA Application No:
(ANDA) 074139
Active Ingredient(s):
CLOBETASOL PROPIONATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for CLOBETASOL PROPIONATE, (ANDA) 074139
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/2/2002
016
Control Supplement
9/28/2001
015
Control Supplement
9/28/2001
014
Labeling
9/28/2001
013
Packaging Addition
5/31/2002
012
Control Supplement
5/31/2002
011
Supplier Addition
12/29/2000
010
Control Supplement
8/18/1999
009
Chemistry
1/7/1998
008
Labeling
6/28/1996
007
Chemistry
8/16/1996
006
Chemistry
8/16/1996
005
Chemistry
8/16/1996
004
Chemistry
8/16/1996
003
Chemistry
12/5/1995
002
Chemistry
3/13/1995
001
Chemistry
8/3/1994
000
Approval
Therapeutic Equivalents
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