NDC 51672-4225 – Bumetanide

Bumetanide 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51672-4225

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213458
Marketed since
July 24, 2023
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
51672-4225-1100 TABLET in 1 BOTTLE (51672-4225-1)Jul 24, 2023

Other Bumetanide products