Potassium Chloride Tablet, Extended Release
Product Images NDC 24979-229

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 24979-229). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image Description (10meq 100c)

Image Description (10meq 100c)
This text contains information about an extended-release tablet of Potassium Chloride, USP with a dosage of 750 mg (equivalent to potassium 10 mEq) per tablet. It provides guidance on dosage adjustment, storage conditions, and patient information regarding excretion in stool. The medication is dispensed in a tight container with a child-resistant closure. The manufacturing details, including the manufacturer and distributor, are also provided. Additionally, it mentions that the FDA-approved acceptance criteria for assay differ from the USP test. The prescription is for 100 tablets, and the lot number and expiration date are also included.*
FDA Label Image

Image Description (8meq 100c)

Image Description (8meq 100c)
This text provides detailed information about extended-release potassium chloride tablets, with each tablet containing 600 mg of potassium (8 mEq). Dosage adjustment is necessary based on individual patient needs, and storage instructions include maintaining the tablets between 20-25°C (68-77°F). The tablets should be dispensed in a tightly closed container with a child-resistant closure. The tablets are not absorbed and may be excreted intact in the stool. The manufacturer is TWi Pharmaceuticals USA, Inc. and they are indicated for prescription-only use. The FDA assay criteria can differ from the USP test. The label also includes the NDC number, lot number, expiration date, and batch information.*
FDA Label Image
Image Description (Logo)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.