DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CETAMIDE
FDA Application No:
(ANDA) 080021
Active Ingredient(s):
SULFACETAMIDE SODIUM
Company:
ALCON
Label History
Labels are not available on this site for CETAMIDE, (ANDA) 080021
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/18/2000
017
Microbiology
3/23/1999
016
Chemistry
12/12/1996
015
Microbiology
4/18/1996
014
Chemistry
4/18/1996
013
Chemistry
8/23/1994
012
Chemistry
8/31/1993
011
Labeling
8/19/1992
010
Chemistry
8/31/1993
009
Labeling
7/5/1991
008
Labeling
3/9/1990
007
Chemistry
9/15/1989
006
Labeling
3/9/1990
005
Chemistry
3/30/1982
001
Chemistry
9/27/1972
000
Approval
Therapeutic Equivalents
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