NDC 72603-889 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72603-889

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
NorthStar Rx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213942
Marketed since
June 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (1)

Package NDCDescriptionSince
72603-889-01100 TABLET in 1 BOTTLE (72603-889-01)Jun 1, 2026

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