Active Ingredient: AMIFOSTINE
Proprietary Name: AMIFOSTINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A204363
Product Number: 001
Approval Date: Jul 17, 2017
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
