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
- 67296-2136_4f790a18-4685-89e3-e063-6294a90ab1a0
- Product NDC
- 67296-2136
- Form
- TABLET
- Composition / generic term
- Furosemide
- Labeler
- Redpharm Drug
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221105
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET in 1 BOTTLE (67296-2136-1) · 67296-2136-1
- 6 TABLET in 1 BOTTLE (67296-2136-2) · 67296-2136-2
- 30 TABLET in 1 BOTTLE (67296-2136-3) · 67296-2136-3
- 7 TABLET in 1 BOTTLE (67296-2136-4) · 67296-2136-4
- 5 TABLET in 1 BOTTLE (67296-2136-5) · 67296-2136-5
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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