Potassium Chloride Tablet, Film Coated, Extended Release
Product Images NDC 65862-987

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 65862-987). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (8 mEq (600 mg) (100 Tablets Bottle))

Label for Potassium Chloride Extended-Release Tablets, USP 600 mg (8 mEq) by Aurobindo Pharma Limited. The film-coated extended-release tablets are for oral use, packaged as 100 tablets. The label includes dosage instructions, storage guidelines, patient information, and distributor details for Aurobindo Pharma USA, Inc.*

FDA Label Image

Package Label-principal Display Panel (8 mEq (600 mg) Blister Carton (20 x 4 Unit-Dose Tablets) Label)

Potassium Chloride Extended-Release Tablets, USP 8 mEq (600 mg) film-coated oral tablets in a carton label. The label states 80 tablets per package (20 x 4 unit-dose) and is marked Rx only. Distributed by Aurobindo Pharma USA, Inc. The package includes dosage and storage instructions and highlights that the product is made in India by Aurobindo Pharma Limited.*

FDA Label Image

Package Label-principal Display Panel (10 mEq (750 mg) (100 Tablets Bottle)

Label for Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq) by Aurobindo Pharma Limited. The label indicates the product is Rx only, contains 100 film-coated extended-release tablets, and provides storage and patient information. It includes a barcode and distributor details for Aurobindo Pharma USA, Inc.*

FDA Label Image

Package Label-principal Display Panel (10 mEq (750 mg) Blister Carton (20 x 4 Unit-Dose Tablets) Label)

Potassium Chloride Extended-Release Tablets, USP 10 mEq (750 mg) film-coated oral tablets. The carton contains 80 tablets (20 x 4 unit-dose) distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions, patient information, and a barcode. The labeler is Aurobindo Pharma Limited; the product is made in India.*

* 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.