NDC 0832-0540 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC0832-0540

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209916
Marketed since
January 30, 2018
Marketing end
September 30, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (0)

Package NDCDescriptionSince

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