NDC 23155-900 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-900

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
July 15, 2025
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
23155-900-01100 TABLET in 1 BOTTLE (23155-900-01)Jul 15, 2025
23155-900-05500 TABLET in 1 BOTTLE (23155-900-05)Jul 15, 2025
23155-900-101000 TABLET in 1 BOTTLE (23155-900-10)Jul 15, 2025

Other Bumetanide products