DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MECLOFENAMATE SODIUM
FDA Application No:
(ANDA) 072262
Active Ingredient(s):
MECLOFENAMATE SODIUM
Company:
SANDOZ
Label History
Labels are not available on this site for MECLOFENAMATE SODIUM, (ANDA) 072262
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/31/1996
003
Labeling
2/10/1995
002
Chemistry
12/21/1992
001
Labeling
11/29/1988
000
Approval
Therapeutic Equivalents
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