Active Ingredient: BUMETANIDE
Proprietary Name: BUMETANIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209724
Product Number: 001
Approval Date: Oct 18, 2017
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS CO GMBH
Marketing Status:
Prescription
Patent and Exclusivity Information