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
- 71610-107_54b54e0a-1488-4e0e-bffe-0980faf6f25b
- Product NDC
- 71610-107
- Form
- TABLET, FILM COATED
- Composition / generic term
- Gemfibrozil
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20061020
- Source listing expiry
- 20261231
Source-listed ingredients
- GEMFIBROZIL — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (71610-107-53) · 71610-107-53
- 90 TABLET, FILM COATED in 1 BOTTLE (71610-107-60) · 71610-107-60
- 180 TABLET, FILM COATED in 1 BOTTLE (71610-107-80) · 71610-107-80
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →