NDC 69238-1489 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69238-1489

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209724
Marketed since
October 18, 2017
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (2)

Package NDCDescriptionSince
69238-1489-1100 TABLET in 1 BOTTLE (69238-1489-1)Oct 18, 2017
69238-1489-5500 TABLET in 1 BOTTLE (69238-1489-5)Oct 18, 2017

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