Active Ingredient: FUROSEMIDE
Proprietary Name: FUROSEMIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018579
Product Number: 001
Approval Date: Nov 30, 1983
Applicant Holder Full Name: AMERICAN REGENT INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
