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
- 17856-3298_5460bc4c-f415-0813-e063-6294a90a3091
- Product NDC
- 17856-3298
- Form
- SOLUTION
- Composition / generic term
- Furosemide
- Labeler
- Atlantic Biologicals Corps
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19870422
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 40 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 mL in 1 CUP (17856-3298-1) · 17856-3298-1
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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