DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BETATREX
FDA Application No:
(NDA) 018862
Active Ingredient(s):
BETAMETHASONE VALERATE
Company:
SAVAGE LABS
Label History
Labels are not available on this site for BETATREX, (NDA) 018862
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/4/1999
010
Labeling
3/7/1996
008
Chemistry
11/7/1988
007
Labeling
10/20/1988
006
Chemistry
10/20/1988
005
Chemistry
5/28/1987
002
Chemistry
5/28/1987
001
Chemistry
8/31/1983
000
Approval
Therapeutic Equivalents
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