Potassium Chloride Tablet, Extended Release
Product Images NDC 63304-987

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 63304-987). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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.

FDA Label Image

1500mg- 100ct (6330498701)

1500mg- 100ct (6330498701)
Potassium Chloride Extended-Release Tablets, USP 1500 mg (20 mEq K) oral tablets. The label indicates a package of 100 tablets. Manufactured by Adare Pharmaceuticals and distributed by Sun Pharmaceutical Industries, Inc. The label includes storage instructions and safety warnings.*
FDA Label Image

1500mg-500ct (6330498705)

1500mg-500ct (6330498705)
Potassium Chloride Extended-Release Tablets, USP 1500 mg (20 mEq potassium) oral tablets in a 500-tablet package. The label shows the product name, strength, dosage form, NDC 63304-987-05, and the labeler Sun Pharmaceutical Industries, Inc. Additional text includes storage instructions and manufacturer details.*
FDA Label Image

1500mg-1000ct (6330498710)

1500mg-1000ct (6330498710)
Label for Potassium Chloride Extended-Release Tablets, USP, 1500 mg (20 mEq potassium), oral dosage form. The label indicates a package size of 1000 tablets, manufactured by Adare Pharmaceuticals, Inc., and distributed by Sun Pharmaceutical Industries, Inc. Includes storage instructions and a barcode with NDC 63304-987.*

* 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.