DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FENOPROFEN CALCIUM
FDA Application No:
(ANDA) 072326
Active Ingredient(s):
FENOPROFEN CALCIUM
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for FENOPROFEN CALCIUM, (ANDA) 072326
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/4/1999
010
Control Supplement
11/4/1999
009
Manufacturing Revision
12/1/1998
008
Chemistry
10/6/1995
007
Chemistry
4/15/1991
006
Chemistry
12/19/1988
005
SBA
3/31/1989
005
Labeling
12/15/1988
003
Chemistry
12/15/1988
002
Chemistry
7/20/1988
001
Other
4/20/1988
000
Approval
Therapeutic Equivalents
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