Active Ingredient: BUMETANIDE
Proprietary Name: BUMEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018226
Product Number: 001
Approval Date: Feb 28, 1983
Applicant Holder Full Name: VALIDUS PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
