Image 1
Chemical structure of potassium citrate hydrate showing the citrate ion complexed with three potassium ions and a water molecule.*
Potassium Citrate Tablet, Extended Release
Product Images NDC 0591-2729
4 FDA label images from Actavis Pharma, Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Citrate (NDC 0591-2729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Actavis Pharma, 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.
Image 2
Label for Potassium Citrate Extended-Release Tablets USP, 5 mEq (540 mg) per tablet, in a 100 count bottle. The tablets are uncoated, tan to yellowish, speckled, round shaped, and designated for extended release. The product is labeled as Rx only and manufactured for Teva Pharmaceuticals by Watson Pharma Private Ltd. Storage instructions and usage notes are also included.*
Image 3
Label for Potassium Citrate Extended-Release Tablets, USP, 10 mEq (1080 mg) per tablet. The label indicates the product contains 100 tablets, is Rx only, and is an extended-release tablet. It lists storage instructions, dosing and pharmacist cautions, and manufacturer details including Watson Pharma Pvt. Ltd. and Teva Pharmaceuticals.*
Image 4
Potassium Citrate Extended-Release Tablets, USP 15 mEq (1620 mg) per tablet label from Actavis Pharma, Inc. for a package of 100 tablets. The label includes dosage information, storage instructions, manufacturer details, and a warning to keep medications out of reach of children. It also features a barcode and serialization code area.*
* 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.
