NDC 0832-0542 – Bumetanide

Bumetanide 2 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC0832-0542

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209916
Marketed since
January 30, 2018
Marketing end
September 30, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (2)

Package NDCDescriptionSince
0832-0542-101000 TABLET in 1 BOTTLE (0832-0542-10)Jan 30, 2018
0832-0542-11100 TABLET in 1 BOTTLE (0832-0542-11)Jan 30, 2018

Recalls mentioning this NDC

Other Bumetanide products