Active Ingredient: DOXORUBICIN HYDROCHLORIDE
Proprietary Name: DOXORUBICIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A200170
Product Number: 002
Approval Date: Oct 28, 2011
Applicant Holder Full Name: MYLAN LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information