Potassium Chloride Tablet, Film Coated, Extended Release
Product Images NDC 68001-518

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 68001-518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

100 Tablet Label (Potassium Fig3)

100 Tablet Label (Potassium Fig3)
This is a description of a prescription drug named Potassium Chloride Extended-Release Tablets. Each film-coated extended-release tablet contains 750 mg of USP Potassium Chloride. Dosage must be adjusted to the individual needs of each patient. The drug should be stored at 20-25°C and should be protected from light and moisture. Patients should be aware that the expended matrix is not absorbed and may be excreted intact in the stool. The drug should be kept out of reach of children. The manufacturer of this drug is APL Healthcare Limited located in Andhra Pradesh, India. The drug was approved by the FDA, but the acceptance criteria for assay differs from the USP test.*

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