United States · FDA National Drug Code directory
RANOLAZINE
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
- 72319-022_163908d8-6b41-4e68-b14c-76faa57c7ac0
- Product NDC
- 72319-022
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- RANOLAZINE
- Labeler
- i3 Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220615
- Source listing expiry
- 20261231
Source-listed ingredients
- RANOLAZINE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72319-022-02) · 72319-022-02
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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