NDC 72162-2195 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2195

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074700
Marketed since
November 21, 1996
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2195-1100 TABLET in 1 BOTTLE (72162-2195-1)Dec 15, 2023

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