NDC 23155-901 – Bumetanide

Bumetanide 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-901

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
23155-901-01100 TABLET in 1 BOTTLE (23155-901-01)Jun 28, 2024
23155-901-05500 TABLET in 1 BOTTLE (23155-901-05)Jun 28, 2024
23155-901-101000 TABLET in 1 BOTTLE (23155-901-10)Jun 28, 2024

Other Bumetanide products