NDC 71335-2556 – Ranolazine

Ranolazine 500 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2556

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213517
Marketed since
June 15, 2022
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
71335-2556-160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2556-1)Jan 23, 2025

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