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
- 71335-2317_14a56e92-68a4-4145-ba70-de5731cf044a
- Product NDC
- 71335-2317
- 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 — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 40 TABLET in 1 BOTTLE (71335-2317-1) · 71335-2317-1
- 30 TABLET in 1 BOTTLE (71335-2317-2) · 71335-2317-2
- 100 TABLET in 1 BOTTLE (71335-2317-3) · 71335-2317-3
- 90 TABLET in 1 BOTTLE (71335-2317-4) · 71335-2317-4
- 60 TABLET in 1 BOTTLE (71335-2317-5) · 71335-2317-5
- 7 TABLET in 1 BOTTLE (71335-2317-6) · 71335-2317-6
- 14 TABLET in 1 BOTTLE (71335-2317-7) · 71335-2317-7
- 180 TABLET in 1 BOTTLE (71335-2317-8) · 71335-2317-8
- 10 TABLET in 1 BOTTLE (71335-2317-9) · 71335-2317-9
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.
Browse United States records →