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
50090-6137_27bb22b8-1b0b-4552-a0be-5b76c2ccf8cc
Product NDC
50090-6137
Form
TABLET
Composition / generic term
bumetanide
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20180501
Source listing expiry
20271231

Source-listed ingredients

  • BUMETANIDE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (50090-6137-0) · 50090-6137-0

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.

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