Potassium Chloride Extended-release Tablet
Product Images NDC 62207-726

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Potassium Chloride Extended-release (NDC 62207-726). 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

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Label for Potassium Chloride Extended-Release Tablets, USP containing 1500 mg strength equivalent to 20 mEq potassium. The label shows a count of 1000 tablets, marked Rx only. Manufactured by Granules India Limited, Hyderabad, India, and for Granules Pharmaceuticals Inc., Chantilly, VA. The label includes dosage and storage instructions and two barcodes.*

FDA Label Image

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Label of Potassium Chloride Extended-Release Tablets, USP showing the 750 mg strength equivalent to 10 mEq of potassium. The label indicates this is a prescription oral tablet, supplied in a package of 1000 tablets. It is manufactured by Granules India Limited and labeled for Granules Pharmaceuticals Inc. Storage, dosage, and safety information is included.*

FDA Label Image

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Potassium Chloride Extended-Release Tablets, USP label for oral tablets containing 750 mg potassium chloride (10 mEq potassium), packaged as 100 tablets. The label includes storage instructions, dosage note, and manufacturer information: Granules India Limited, Hyderabad, India, and Granules Pharmaceuticals Inc., Chantilly, VA. The label cautions to keep out of reach of children and store in a tight, light-resistant container.*

FDA Label Image

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Label for Potassium Chloride Extended-Release Tablets, USP, 750 mg strength, oral dosage form, manufactured by Granules India Ltd. The label states this is a prescription drug available in a bottle containing 500 tablets. It includes storage instructions, dosage information, a barcode, and manufacturer details for Granules Pharmaceuticals Inc. in Chantilly, VA.*

FDA Label Image

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Label for Potassium Chloride Extended-Release Tablets, USP containing 750 mg potassium chloride per tablet with 10 mEq potassium. The oral extended-release tablet package contains 90 tablets. Manufactured by Granules India Limited and for Granules Pharmaceuticals Inc. Directions include storage instructions and dosage warnings, along with child-resistant container details. The label includes NDC 62207-726-57 and barcodes.*

FDA Label Image

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Potassium Chloride Extended-Release Tablets, USP 1500 mg tablet label, emphasizing 20 mEq potassium, prescription only. The label indicates packaging contains 100 tablets, manufactured by Granules India Limited in Hyderabad, India, with distribution by Granules Pharmaceuticals Inc., Chantilly, VA. It specifies extended-release formulation and storage conditions.*

FDA Label Image

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Potassium Chloride Extended-Release Tablets USP label showing 20 mEq potassium strength, with package size of 500 tablets. Label includes storage instructions, manufacturer Granules India Limited, and barcode. The label is for oral tablets and indicates Rx only.*

FDA Label Image

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Potassium Chloride Extended-Release Tablets, USP 1500 mg strength label for oral tablets, containing 20 mEq potassium per tablet. The label indicates a package size of 800 tablets and is manufactured by Granules India Limited, India, and Granules Pharmaceuticals Inc., Chantilly, VA. The label also includes storage instructions and warns to keep out of reach of children.*

FDA Label Image

Kcl-er-20meq-90label-jpg (Kcl Er 20meq 90label Jpg)

Potassium Chloride Extended-Release Tablets, USP 1500 mg with 20 mEq potassium strength, oral dosage form. The label indicates 90 tablets per container, manufactured by Granules India Limited and labeled for Granules Pharmaceuticals Inc. Storage instructions and dosage adjustment notes are visible along with a barcode.*

* 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.