Active Ingredient: CEPHALOTHIN SODIUM
Proprietary Name: CEPHALOTHIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A062666
Product Number: 002
Approval Date: Jun 10, 1987
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information