Potassium Chloride Capsule, Extended Release
Product Images NDC 70010-148

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 70010-148). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules Pharmaceuticals 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

Kcl-500mg-100label-jpg (Kcl 500mg 100label Jpg)

Label for Potassium Chloride Extended-Release Capsules USP, 600 mg (8 mEq), 100 capsules per container. The label indicates the capsules release potassium chloride over 8 to 10 hours. Manufactured by Granules India Limited and labeled for Granules Pharmaceuticals Inc. Storage instructions, usage dosage reference, and child-resistant container warning are included. The label also features barcodes and manufacturing details.*

FDA Label Image

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

Potassium Chloride Extended-Release Capsules USP label showing 10 mEq K (750 mg) strength in a 100 capsule package. The label includes storage instructions, child-resistant container requirement, manufacturing information by Granules India Limited, and the product is for oral use. The label also features barcodes and a red warning box for strength.*

FDA Label Image

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

Potassium Chloride Extended-Release Capsules, USP 10 mEq K (750 mg), 500 count bottle label. The label indicates the capsules are manufactured by Granules India Limited and for Granules Pharmaceuticals Inc., Chantilly, VA. Storage instructions specify controlled room temperature. The label includes product NDC 70010-148-05 and emphasizes dispensing in a child-resistant container.*

* 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.