Active Ingredient: DAUNORUBICIN HYDROCHLORIDE
Proprietary Name: CERUBIDINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AP
Application Number: A064103
Product Number: 001
Approval Date: Feb 3, 1995
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information