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
- 63561-0164_54741cba-d4ee-617e-e063-6294a90ad1eb
- Product NDC
- 63561-0164
- Form
- TABLET
- Composition / generic term
- FUROSEMIDE
- Labeler
- Granulation Technology, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20251218
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (63561-0164-1) · 63561-0164-1
- 1000 TABLET in 1 BOTTLE (63561-0164-2) · 63561-0164-2
- 90 TABLET in 1 BOTTLE (63561-0164-9) · 63561-0164-9
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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