NDC 16571-679 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16571-679

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Rising Pharma Holdings, Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212019
Marketed since
June 3, 2024
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (1)

Package NDCDescriptionSince
16571-679-01100 TABLET in 1 BOTTLE (16571-679-01)Jun 3, 2024

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