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
- 82804-286_ae7dd557-f7a1-4d5a-b80e-3ca3a6e4943b
- Product NDC
- 82804-286
- Form
- TABLET
- Composition / generic term
- bumetanide
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240603
- Source listing expiry
- 20271231
Source-listed ingredients
- BUMETANIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (82804-286-30) · 82804-286-30
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 →