Active Ingredient: DAUNORUBICIN HYDROCHLORIDE
Proprietary Name: CERUBIDINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050484
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WYETH AYERST RESEARCH
Marketing Status:
Discontinued
Patent and Exclusivity Information