NDC 0781-8099 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0781-8099

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Sandoz Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074700
Marketed since
June 3, 2026
Listing expires
December 31, 2027
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (2)

Package NDCDescriptionSince
0781-8099-01100 TABLET in 1 BOTTLE (0781-8099-01)Jun 3, 2026
0781-8099-05500 TABLET in 1 BOTTLE (0781-8099-05)Jun 3, 2026

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