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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 209445

FETROJA (CEFIDEROCOL SULFATE TOSYLATE)
EQ 1GM BASE/VIAL
Marketing Status: Prescription
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
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