Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: CEFOXITIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A065238
Product Number: 001
Approval Date: Mar 12, 2010
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:
Prescription
Patent and Exclusivity Information