Warfarin Sodium Tablet
Product Images NDC 70518-2717

3 FDA label images from Remedyrepack Inc. · 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 Warfarin Sodium (NDC 70518-2717). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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.

Product Images & Figures Index

FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Warfarin Sodium 7.5 mg oral tablets in a quantity of 100. The label shows the strength and dosage form prominently with the brand Remedy Repack and labeler RemedyRepack Inc. It includes NDC 70518-2717-00 and repackaging information by RemedyRepack Inc., Indiana, PA. Manufacturer is Amneal Pharma, Bridgewater, NJ. The label also advises to see the package insert for directions and to store tablets at 20-25°C with permitted excursions.*
FDA Label Image

Mm2 (Warfarin Sodium 7.5mg 70518 2717 01)

Mm2 (Warfarin Sodium 7.5mg 70518 2717 01)
Warfarin Sodium 7.5 mg tablet packaging label showing a single oral dosage form. The label includes the remody repack logo, NDC number 70518-2717-01, manufacturing information for Amneal Pharma, and repackaging details from RemedyRepack Inc. The label also notes storage conditions and a caution to keep medication out of children's reach.*
FDA Label Image

474ff828-figure-01 (Warfarin Sodium Tablets Usp 1)

474ff828-figure-01 (Warfarin Sodium Tablets Usp 1)
Chemical structure diagram of Warfarin, representing its molecular framework with labeled atoms and bonds.*

* 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.