DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VANCENASE AQ
FDA Application No:
(NDA) 019589
Active Ingredient(s):
BECLOMETHASONE DIPROPIONATE MONOHYDRATE
Company:
SCHERING
Label History
Labels are not available on this site for VANCENASE AQ, (NDA) 019589
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/30/2000
008
Control Supplement
6/15/1995
004
Package Change
9/2/1993
003
Control Supplement
9/2/1993
002
Manufacturing Change or Addition
12/15/1988
001
Labeling Revision
12/23/1987
000
Approval
Therapeutic Equivalents
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