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
- 72162-2633_80d48f46-53e7-428b-b03c-e22b7e0305d8
- Product NDC
- 72162-2633
- Form
- INJECTION
- Composition / generic term
- Bumetanide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220806
- Source listing expiry
- 20271231
Source-listed ingredients
- BUMETANIDE — .25 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (72162-2633-2) / 4 mL in 1 VIAL (72162-2633-4) · 72162-2633-2
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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