Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050581

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MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER (CEFOXITIN SODIUM)
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050581
Product Number: 003
Approval Date: Sep 20, 1984
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER (CEFOXITIN SODIUM)
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050581
Product Number: 004
Approval Date: Sep 20, 1984
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (CEFOXITIN SODIUM)
EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050581
Product Number: 002
Approval Date: Sep 20, 1984
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (CEFOXITIN SODIUM)
EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N050581
Product Number: 001
Approval Date: Sep 20, 1984
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information