Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: KEFUROX IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 750MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A062590
Product Number: 001
Approval Date: Jan 10, 1986
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information