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Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: KEFUROX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1.5GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A062592
Product Number: 002
Approval Date: Jan 10, 1986
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: KEFUROX
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 750MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A062592
Product Number: 001
Approval Date: Jan 10, 1986
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
