Active Ingredient: DAUNORUBICIN HYDROCHLORIDE
Proprietary Name: DAUNORUBICIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065034
Product Number: 001
Approval Date: Nov 20, 2001
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
