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
- 71335-0842_14d6a850-12a9-4c10-bd7c-1c1acf500d56
- Product NDC
- 71335-0842
- Form
- TABLET
- Composition / generic term
- furosemide
- Labeler
- Bryant Ranch Prepack
- 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
- 40 TABLET in 1 BOTTLE (71335-0842-1) · 71335-0842-1
- 30 TABLET in 1 BOTTLE (71335-0842-2) · 71335-0842-2
- 100 TABLET in 1 BOTTLE (71335-0842-3) · 71335-0842-3
- 90 TABLET in 1 BOTTLE (71335-0842-4) · 71335-0842-4
- 60 TABLET in 1 BOTTLE (71335-0842-5) · 71335-0842-5
- 7 TABLET in 1 BOTTLE (71335-0842-6) · 71335-0842-6
- 14 TABLET in 1 BOTTLE (71335-0842-7) · 71335-0842-7
- 180 TABLET in 1 BOTTLE (71335-0842-8) · 71335-0842-8
- 10 TABLET in 1 BOTTLE (71335-0842-9) · 71335-0842-9
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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