Ranolazine Tablet, Extended Release
Product Images NDC 70771-1500

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 70771-1500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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 (82ddee01 7ba8 4657 Aaca Ef1335278215 01)

Structure (82ddee01 7ba8 4657 Aaca Ef1335278215 01)
Chemical structure of Ranolazine, shown as a molecular diagram with labeled bonds and substituents, illustrating the compound's chemical connectivity and functional groups.*
FDA Label Image

Container Label 500mg (82ddee01 7ba8 4657 Aaca Ef1335278215 02)

Container Label 500mg (82ddee01 7ba8 4657 Aaca Ef1335278215 02)
Label for Ranolazine Extended-Release Tablets 500 mg, oral dosage form. The label states "Swallow tablets whole; do not crush, break, or chew" and indicates a quantity of 60 tablets, prescription only. It is manufactured by Cadila Healthcare Ltd., India. Storage instructions and NDC number 70771-1499-6 are also present.*
FDA Label Image

Container Label 1000mg (82ddee01 7ba8 4657 Aaca Ef1335278215 03)

Container Label 1000mg (82ddee01 7ba8 4657 Aaca Ef1335278215 03)
Ranolazine Extended-Release Tablets 1000 mg oral dosage form label, showing a package containing 60 tablets. The label includes storage instructions, warnings to keep out of children's reach, and directions to swallow tablets whole without crushing, breaking, or chewing. Manufactured by Cadila Healthcare Ltd., India, with labeler Zydus Lifesciences Limited mentioned in product data.*

* 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.