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) 062480
Active Ingredient(s):
GENTAMICIN SULFATE
Company:
NOVARTIS
Label History
Labels are not available on this site for GENTACIDIN, (ANDA) 062480
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2001
009
Facility Addition
2/12/1999
007
Labeling
8/22/1995
006
Chemistry
5/5/1994
005
Labeling
6/10/1994
004
Microbiology
9/30/1994
003
Chemistry
8/19/1993
002
Labeling
3/30/1984
000
Approval
Therapeutic Equivalents
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