Potassium Chloride Extended-release Tablet, Extended Release
Product Images NDC 63304-076

3 FDA label images from Sun Pharmaceutical Industries, Inc. · 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 Extended-release (NDC 63304-076). 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

Pdp-750mg-100count (Image 01)

Pdp-750mg-100count (Image 01)
Potassium Chloride Extended-Release Tablets USP 750 mg (10 mEq K) label from Sun Pharmaceutical Industries, Inc. The label includes dosage strength, extended-release tablet form, NDC number 63304-076-01, storage instructions, manufacturing and distribution information, and a barcode. The package size indicated is 100 tablets, Rx only.*
FDA Label Image

Pdp-750mg-500count (Image 02)

Pdp-750mg-500count (Image 02)
Label for Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq K) by Sun Pharmaceutical Industries, Inc. The label includes dosage form as extended-release tablets, prescription only, and a package count of 500 tablets. It provides storage instructions and manufacturer and distributor information.*
FDA Label Image

Pdp-750mg-1000count (Image 03)

Pdp-750mg-1000count (Image 03)
Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq K) oral extended-release tablets by Sun Pharmaceutical Industries, Inc. The label states 1000 tablets per container and indicates prescription use only (Rx only). Storage and dispensing instructions, manufacturer and distributor information, NDC 63304-076, and barcode are also visible.*

* 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.