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
- 23155-900_ee0c44ac-10ca-4d9b-98f0-1342fc97dd39
- Product NDC
- 23155-900
- Form
- TABLET
- Composition / generic term
- bumetanide
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250715
- 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 (23155-900-01) · 23155-900-01
- 500 TABLET in 1 BOTTLE (23155-900-05) · 23155-900-05
- 1000 TABLET in 1 BOTTLE (23155-900-10) · 23155-900-10
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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