NDC 71610-518 – Ranolazine

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

Human Prescription Drug

Product NDC71610-518

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212781
Marketed since
October 27, 2020
Listing expires
December 31, 2026
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (2)

Package NDCDescriptionSince
71610-518-421800 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-518-42)Apr 1, 2024
71610-518-833600 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-518-83)Jan 22, 2021

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