Potassium Chloride Capsule, Extended Release
Product Images NDC 62207-915

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 62207-915). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Ltd, 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

Kcl-600mg-500label-jpg (Kcl 600mg 500label Jpg)

Kcl-600mg-500label-jpg (Kcl 600mg 500label Jpg)
Label for Potassium Chloride Extended-Release Capsules, USP 600 mg (8 mEq K) showing a 500 capsule package. The label indicates the drug is manufactured by Granules India Limited and distributed by Granules Pharmaceuticals Inc. The label includes storage instructions, dosage form as oral extended-release capsules, and a barcode.*
FDA Label Image

Kcl-750mg-100label-jpg (Kcl 750mg 100label Jpg)

Kcl-750mg-100label-jpg (Kcl 750mg 100label Jpg)
Potassium Chloride Extended-Release Capsules, USP 10 mEq K (750 mg), 100 capsules in a child-resistant container. The label indicates the product is manufactured by Granules India Limited, Hyderabad, India, for Granules Pharmaceuticals Inc. Dosage form is extended-release capsules for oral use.*
FDA Label Image

Kcl-750mg-500label-jpg (Kcl 750mg 500label Jpg)

Kcl-750mg-500label-jpg (Kcl 750mg 500label Jpg)
Label for Potassium Chloride Extended-Release Capsules, USP 10 mEq (750 mg), oral extended-release capsules. The label indicates a package size of 500 capsules and is manufactured by Granules India Limited, India, for Granules Pharmaceuticals Inc., Chantilly, VA. It includes storage instructions and a barcode.*
FDA Label Image

Kcl-er-600mg-1000s-label1-jpg (Kcl Er 600mg 1000s Label1 Jpg)

Kcl-er-600mg-1000s-label1-jpg (Kcl Er 600mg 1000s Label1 Jpg)
Potassium Chloride Extended-Release Capsules, USP 600 mg (8 mEq) in bulk container packaging. The label states it contains 1000 capsules and is for prescription use only. Manufactured by Granules India Limited and Granules Pharmaceuticals Inc. The label includes storage instructions and a barcode.*
FDA Label Image

Kcl-er-600mg-100s-label-jpg (Kcl Er 600mg 100s Label Jpg)

Kcl-er-600mg-100s-label-jpg (Kcl Er 600mg 100s Label Jpg)
Label for Potassium Chloride Extended-Release Capsules USP, 8 mEq K (600 mg), oral extended-release capsules. The container holds 100 capsules and is labeled Rx only. Manufactured by Granules India Limited, Hyderabad, India, for Granules Pharmaceuticals Inc., Chantilly, VA. Storage instructions and a barcode are also present.*
FDA Label Image

Kcl-er-750mg-1000s-label1-jpg (Kcl Er 750mg 1000s Label1 Jpg)

Kcl-er-750mg-1000s-label1-jpg (Kcl Er 750mg 1000s Label1 Jpg)
Label for Potassium Chloride Extended-Release Capsules, USP 10 mEq K (750 mg), in a bulk container with 1000 capsules. The label includes storage instructions, manufacturer information (Granules India Limited, Hyderabad, India), and mentions dispensing in a child-resistant container. It is marked Rx only and displays a barcode.*
FDA Label Image

Kcl-er-750mg-90s-label-jpg (Kcl Er 750mg 90s Label Jpg)

Kcl-er-750mg-90s-label-jpg (Kcl Er 750mg 90s Label Jpg)
Label for Potassium Chloride Extended-Release Capsules USP containing 10 mEq (750 mg) of potassium chloride, presented in a bottle of 90 capsules. The label states the medication is manufactured by Granules India Limited in India and labeled for Granules Pharmaceuticals Inc., Chantilly, VA. It includes storage instructions, dispensing requirements for a child-resistant container, and dosage guidance to refer to prescribing information.*

* 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.