United States · FDA National Drug Code directory
Gemfibrozil
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
- 51655-143_48c3ec58-2075-5cc3-e063-6394a90aaffa
- Product NDC
- 51655-143
- Form
- TABLET
- Composition / generic term
- Gemfibrozil
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170814
- Source listing expiry
- 20271231
Source-listed ingredients
- GEMFIBROZIL — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET in 1 BOTTLE, PLASTIC (51655-143-25) · 51655-143-25
- 90 TABLET in 1 BOTTLE, PLASTIC (51655-143-26) · 51655-143-26
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-143-52) · 51655-143-52
- 180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83) · 51655-143-83
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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