Active Ingredient: DOXORUBICIN HYDROCHLORIDE
Proprietary Name: DOXORUBICIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A063336
Product Number: 004
Approval Date: Feb 28, 1995
Applicant Holder Full Name: PHARMACHEMIE BV
Marketing Status:
Discontinued
Patent and Exclusivity Information