DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
FDA Application No:
(ANDA) 062488
Active Ingredient(s):
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Company:
ALCON UNIVERSAL
Label History
Labels are not available on this site for NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE, (ANDA) 062488
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/24/2002
021
Labeling
12/23/2002
020
Microbiology
12/24/2002
018
Control Supplement
12/24/2002
017
Supplier Addition
12/24/2002
016
Package Change
12/24/2002
015
Facility Addition
12/24/2002
014
Manufacturing Revision
2/19/1999
012
Microbiology
2/2/1999
011
Microbiology
4/16/1996
010
Chemistry
5/25/1994
008
Labeling in Effect
3/14/1994
007
Chemistry
11/18/1992
006
Labeling
2/28/1991
005
Labeling
1/10/1989
004
Chemistry
1/27/1989
003
Chemistry
11/6/1985
000
Approval
Review
There are no Therapeutic Equivalents
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