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
- 71335-2319_bf3ea890-deb2-4839-9cfe-062f8afec109
- Product NDC
- 71335-2319
- Form
- TABLET
- Composition / generic term
- Furosemide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221105
- Source listing expiry
- 20261231
Source-listed ingredients
- FUROSEMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (71335-2319-0) · 71335-2319-0
- 30 TABLET in 1 BOTTLE (71335-2319-1) · 71335-2319-1
- 90 TABLET in 1 BOTTLE (71335-2319-2) · 71335-2319-2
- 60 TABLET in 1 BOTTLE (71335-2319-3) · 71335-2319-3
- 100 TABLET in 1 BOTTLE (71335-2319-4) · 71335-2319-4
- 7 TABLET in 1 BOTTLE (71335-2319-5) · 71335-2319-5
- 28 TABLET in 1 BOTTLE (71335-2319-6) · 71335-2319-6
- 14 TABLET in 1 BOTTLE (71335-2319-7) · 71335-2319-7
- 10 TABLET in 1 BOTTLE (71335-2319-8) · 71335-2319-8
- 20 TABLET in 1 BOTTLE (71335-2319-9) · 71335-2319-9
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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