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
- 81469-222_25bc351d-4705-4d81-9d44-ac191ec15a34
- Product NDC
- 81469-222
- Form
- TABLET
- Composition / generic term
- Bumetanide
- Labeler
- First Nation Group, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260219
- Source listing expiry
- 20271231
Source-listed ingredients
- BUMETANIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (81469-222-01) · 81469-222-01
- 500 TABLET in 1 BOTTLE (81469-222-05) · 81469-222-05
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →