High Outlier
Strength
2 mg/1
Manufacturer
Zydus Pharmaceuticals (USA) Inc.NDC
68382052701
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
6/18/2025
Active Ingredients
BUMETANIDEApproval Type
Generic (ANDA)
FDA Application
ANDA202900On Market Since
5/1/2018
Pharmacological Classes
Increased Diuresis at Loop of Henle
Loop Diuretic
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