DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GENTAMICIN SULFATE
FDA Application No:
(ANDA) 062251
Active Ingredient(s):
GENTAMICIN SULFATE
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for GENTAMICIN SULFATE, (ANDA) 062251
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/23/2001
028
Control Supplement
7/23/2001
027
Facility Addition
7/23/2001
026
Supplier Addition
10/14/1999
025
Control Supplement
2/11/1999
024
Chemistry
2/3/1994
021
Chemistry
9/16/1993
020
Chemistry
11/18/1991
019
Chemistry
5/17/1991
018
Chemistry
5/31/1991
017
Chemistry
2/8/1991
016
Chemistry
11/19/1990
015
Chemistry
7/12/1988
014
Chemistry
2/22/1988
013
Chemistry
5/22/1987
011
Chemistry
6/5/1980
000
Approval
Therapeutic Equivalents
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