DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VASOCIDIN
FDA Application No:
(NDA) 018988
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Company:
NOVARTIS
Label History
Labels are not available on this site for VASOCIDIN, (NDA) 018988
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/26/2000
009
Manufacturing Change or Addition
11/7/2000
008
Control Supplement
6/8/1995
006
Labeling Revision
5/9/1996
005
Control Supplement
1/10/1992
003
Labeling Revision
8/26/1988
000
Approval
There are no Therapeutic Equivalents
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