Potassium Citrate Tablet, Extended Release
Product Images NDC 65841-537

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Citrate (NDC 65841-537). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

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Chemical structure diagram of potassium citrate monohydrate showing the citrate ion bonded to three potassium ions (COOK) and a water molecule (H2O).*

FDA Label Image

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Potassium Citrate Extended-Release Tablets USP 5 mEq (540 mg per tablet) packaging label. The label indicates 100 tablets in the container, Rx only, manufactured by Cadila Healthcare Ltd, Baddi, India. The tablet is described as tan, yellowish, round, biconvex, uncoated, with '536' debossed on one side. Storage and dispensing information is also included.*

FDA Label Image

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Label for Potassium Citrate Extended-Release Tablets USP 10 mEq (1080 mg per tablet) in a 100 tablet bottle by Zydus Pharmaceuticals. The tablet is tan to yellowish, oval-shaped, biconvex, uncoated, and marked with '537.' The label includes storage instructions and cautions to keep the drug out of children's reach. Manufactured by Cadila Healthcare Ltd., Baddi, India.*

FDA Label Image

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Potassium Citrate Extended-Release Tablets USP 15 mEq (1620 mg per tablet) oral tablets in a 100-tablet container. The tan to yellowish, oblong, biconvex tablets are debossed with "538" on one side. Label includes storage instructions, dispensing information, and is labeled Rx only. Manufactured by Cadila Healthcare Ltd., 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.