United States · FDA National Drug Code directory

Bumetanide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
42799-119_462dc93e-f284-3a48-e063-6394a90a7ce1
Product NDC
42799-119
Form
TABLET
Composition / generic term
Bumetanide
Labeler
Edenbridge Pharmaceuticals LLC.
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20151015
Source listing expiry
20261231

Source-listed ingredients

  • BUMETANIDE — .5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (42799-119-01) · 42799-119-01

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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