United States · FDA National Drug Code directory
Furosemide
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
- 0615-8369_fb99ad62-fc5e-4eab-9f63-20246541729c
- Product NDC
- 0615-8369
- Form
- TABLET
- Composition / generic term
- furosemide
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040326
- Source listing expiry
- 20261231
Source-listed ingredients
- FUROSEMIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BLISTER PACK (0615-8369-05) · 0615-8369-05
- 7 TABLET in 1 BLISTER PACK (0615-8369-07) · 0615-8369-07
- 14 TABLET in 1 BLISTER PACK (0615-8369-14) · 0615-8369-14
- 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8369-30) / 5 TABLET in 1 BLISTER PACK · 0615-8369-30
- 30 TABLET in 1 BLISTER PACK (0615-8369-39) · 0615-8369-39
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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