NDC 72319-021 – Ranolazine

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

Human Prescription Drug

Product NDC72319-021

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
i3 Pharmaceuticals, LLC
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
72319-021-0260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72319-021-02)Jun 15, 2022

Other Ranolazine products