NDC 76282-799 – Bumetanide

Bumetanide 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76282-799

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212931
Marketed since
March 1, 2025
Listing expires
December 31, 2027
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (2)

Package NDCDescriptionSince
76282-799-01100 TABLET in 1 BOTTLE (76282-799-01)Mar 1, 2025
76282-799-05500 TABLET in 1 BOTTLE (76282-799-05)Mar 1, 2025

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