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: 60687-384_21374d66-9881-6023-e063-6394a90a39d2
Product NDC: 60687-384
Form: TABLET
Composition / generic term: Bumetanide
Labeler: American Health Packaging
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20180802
Source listing expiry: 20261231

Source-listed ingredients

BUMETANIDE — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11) · 60687-384-01
50 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11) · 60687-384-65

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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