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Active Ingredient: ROMIDEPSIN
Proprietary Name: ROMIDEPSIN
Dosage Form; Route of Administration: POWDER; INTRAVENOUS
Strength: 10MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A206254
Product Number: 001
Approval Date: Oct 12, 2021
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
