DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 050581
Active Ingredient(s):
CEFOXITIN SODIUM
Company:
MERCK
Label History
Labels are not available on this site for MEFOXIN IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 050581
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/27/1997
020
Supplement
Review
Therapeutic Equivalents
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