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
- 66267-436_1fa6f6ca-cf67-49fd-e063-6394a90a73f2
- Product NDC
- 66267-436
- Form
- TABLET
- Composition / generic term
- Gemfibrozil
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160708
- Source listing expiry
- 20261231
Source-listed ingredients
- GEMFIBROZIL — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (66267-436-30) · 66267-436-30
- 60 TABLET in 1 BOTTLE (66267-436-60) · 66267-436-60
- 180 TABLET in 1 BOTTLE (66267-436-92) · 66267-436-92
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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