Potassium Chloride Tablet, Film Coated, Extended Release
Product Images NDC 70518-2964

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 Potassium Chloride (NDC 70518-2964). 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.

FDA Label Image

Mm2 (Potassium Chloride 10meq (750mg) 70518 2964 01)

Mm2 (Potassium Chloride 10meq (750mg) 70518 2964 01)
Potassium Chloride extended-release 10 mEq (750 mg) film-coated tablets packaging label showing a quantity of 90 tablets. The label includes NDC number 70518-2964-01, manufacturer Aurobindo Pharma Ltd., and repackager RemedyRepack Inc., with storage instructions and a QR code visible.*
FDA Label Image

Potassium Chloride 10meq (750mg) 70518 2964 02

Potassium Chloride 10meq (750mg) 70518 2964 02
Potassium Chloride extended-release 750 mg (10mEq) film-coated tablets packaging label showing a quantity of 100 tablets. The label includes the NDC number 70518-2964-02, manufacturer Aurobindo Pharma Ltd., and repackager RemedyRepack Inc. It notes storage instructions and cautions to keep medication out of children's reach.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Potassium Chloride extended-release tablet 750 mg (10 mEq), film coated. The package contains 30 tablets. Manufactured by Aurobindo Pharma Ltd., India, and repackaged by RemedyRepack Inc. Includes a QR code and directions to see package insert for use.*

* 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.