Active Ingredient: CISPLATIN
Proprietary Name: CISPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074713
Product Number: 001
Approval Date: Nov 14, 2000
Applicant Holder Full Name: BEDFORD LABORATORIES DIV BEN VENUE LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
