NDC 69367-294 – Ranolazine

Ranolazine 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC69367-294

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211829
Marketed since
August 24, 2021
Listing expires
December 31, 2026
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (1)

Package NDCDescriptionSince
69367-294-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69367-294-60)Aug 24, 2021

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