Strength
2 mg/1
Manufacturer
Sandoz Inc.NDC
00185013001
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
BUMETANIDEApproval Type
Generic (ANDA)
FDA Application
ANDA074700On Market Since
11/21/1996
Pharmacological Classes
Increased Diuresis at Loop of Henle
Loop Diuretic
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