Active Ingredient: CEFIDEROCOL SULFATE TOSYLATE
Proprietary Name: FETROJA
Dosage Form; Route of Administration: POWDER; INTRAVENOUS
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N209445
Product Number: 001
Approval Date: Nov 14, 2019
Applicant Holder Full Name: SHIONOGI INC
Marketing Status:
Prescription
Patent and Exclusivity Information