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
- 83980-002_2ef79eb1-61e5-4697-9292-336ca5cf5116
- Product NDC
- 83980-002
- Form
- TABLET
- Composition / generic term
- Furosemide
- Labeler
- Ipca Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240603
- Source listing expiry
- 20261231
Source-listed ingredients
- FUROSEMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (83980-002-01) · 83980-002-01
- 1000 TABLET in 1 BOTTLE (83980-002-10) · 83980-002-10
- 10 TABLET in 1 BOTTLE (83980-002-97) · 83980-002-97
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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