Product Details for NDA 050637
ZEFAZONE (CEFMETAZOLE SODIUM)
EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CEFMETAZOLE SODIUM
Proprietary Name: ZEFAZONE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050637
Product Number: 001
Approval Date: Dec 11, 1989
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
ZEFAZONE (CEFMETAZOLE SODIUM)
Proprietary Name: ZEFAZONE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050637
Product Number: 001
Approval Date: Dec 11, 1989
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CEFMETAZOLE SODIUM
Proprietary Name: ZEFAZONE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050637
Product Number: 002
Approval Date: Dec 11, 1989
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ZEFAZONE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N050637
Product Number: 002
Approval Date: Dec 11, 1989
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information