Active Ingredient: FUROSEMIDE
Proprietary Name: FUROSEMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: N018823
Product Number: 001
Approval Date: Nov 10, 1983
Applicant Holder Full Name: HIKMA PHARMACEUTICALS INTERNATIONAL LTD
Marketing Status:
Prescription
Patent and Exclusivity Information