Active Ingredient: CEFUROXIME SODIUM
Proprietary Name: CEFUROXIME SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAMUSCULAR, INTRAVENOUS
Strength: EQ 750MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065001
Product Number: 001
Approval Date: May 30, 2001
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information