DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GENTACIDIN
FDA Application No:
(ANDA) 062501
Active Ingredient(s):
GENTAMICIN SULFATE
Company:
NOVARTIS
Label History
Labels are not available on this site for GENTACIDIN, (ANDA) 062501
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/3/1996
005
Chemistry
7/3/1996
004
Chemistry
12/15/1995
003
Chemistry
12/9/1997
002
Chemistry
6/12/1992
001
Labeling
7/26/1984
000
Approval
Therapeutic Equivalents
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