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Active Ingredient: EPIRUBICIN HYDROCHLORIDE
Proprietary Name: EPIRUBICIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML (2MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A065411
Product Number: 001
Approval Date: Aug 20, 2007
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: EPIRUBICIN HYDROCHLORIDE
Proprietary Name: EPIRUBICIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/25ML (2MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A065411
Product Number: 002
Approval Date: Aug 20, 2007
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
