DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BETAMETHASONE VALERATE
FDA Application No:
(ANDA) 070051
Active Ingredient(s):
BETAMETHASONE VALERATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for BETAMETHASONE VALERATE, (ANDA) 070051
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/31/2001
017
Control Supplement
5/30/2001
016
Control Supplement
12/29/2000
015
Control Supplement
9/13/1996
014
Chemistry
9/13/1996
013
Chemistry
9/13/1996
012
Chemistry
9/13/1996
011
Chemistry
6/28/1996
010
Chemistry
2/7/1996
009
Chemistry
6/10/1996
008
Chemistry
6/10/1996
007
Chemistry
4/15/1994
006
Labeling
1/29/1993
005
Chemistry
9/11/1989
004
Chemistry
7/29/1992
003
Labeling
10/10/1984
000
Approval
Therapeutic Equivalents
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