Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N065214
Product Number: 001
Approval Date: Mar 10, 2006
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information