DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MEFOXIN
FDA Application No:
(ANDA) 062757
Active Ingredient(s):
CEFOXITIN SODIUM
Company:
MERCK
Original Approval or Tentative Approval Date:
January 8, 1987
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MEFOXIN
CEFOXITIN SODIUM
EQ 1GM BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
MEFOXIN
CEFOXITIN SODIUM
EQ 2GM BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
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