Ranolazine Tablet, Extended Release
Product Images NDC 72578-064

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ranolazine (NDC 72578-064). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona Pharmaceuticals Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structure (9c376fb6 5d19 4977 B152 0db8d2664c2d 01)

Structure (9c376fb6 5d19 4977 B152 0db8d2664c2d 01)
Chemical structure of ranolazine, depicting its molecular arrangement including aromatic rings, amide and ether groups, consistent with the active ingredient ranolazine.*
FDA Label Image

Container Label 500mg (9c376fb6 5d19 4977 B152 0db8d2664c2d 02)

Container Label 500mg (9c376fb6 5d19 4977 B152 0db8d2664c2d 02)
Label for Ranolazine Extended-Release Tablets 500 mg oral tablets. The label indicates 60 tablets per container, manufactured by Cadila Healthcare Ltd., India, and distributed by Viona Pharmaceuticals Inc. Instructions note tablets should not be crushed or broken, with storage guidelines and Rx only status.*
FDA Label Image

Container Label 1000mg (9c376fb6 5d19 4977 B152 0db8d2664c2d 03)

Container Label 1000mg (9c376fb6 5d19 4977 B152 0db8d2664c2d 03)
Ranolazine Extended-Release Tablets 1000 mg, oral extended-release tablets by Viona Pharmaceuticals Inc. The package contains 60 tablets and is labeled Rx only. The label instructs swallowing tablets whole and notes storage at controlled room temperature. Manufactured by Cadila Healthcare Ltd., India, and distributed by Viona Pharmaceuticals Inc., Cranford, NJ.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.