NDC 23155-902 – Bumetanide

Bumetanide 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-902

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074225
Marketed since
June 28, 2024
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (3)

Package NDCDescriptionSince
23155-902-01100 TABLET in 1 BOTTLE (23155-902-01)Jun 28, 2024
23155-902-05500 TABLET in 1 BOTTLE (23155-902-05)Jun 28, 2024
23155-902-101000 TABLET in 1 BOTTLE (23155-902-10)Jun 28, 2024

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