Potassium Chloride Tablet, Extended Release
Product Images NDC 31722-133

3 FDA label images from Camber Pharmaceuticals, 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 (NDC 31722-133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

10 Meq K- 100s Count (10 Meq K 100s)

10 Meq K- 100s Count (10 Meq K 100s)
Potassium Chloride Extended-Release Tablets, USP 750 mg (10 mEq potassium) oral tablets in a 100-count prescription bottle label. Manufactured by Ascent Pharmaceuticals, Inc. and Camber Pharmaceuticals, Inc. The label includes dosing information, storage instructions, and a barcode.*
FDA Label Image

15 Meq K- 100s Count (15 Meq K 100s)

15 Meq K- 100s Count (15 Meq K 100s)
Label for Potassium Chloride Extended-Release Tablets, USP 1125 mg (15 mEq) by Camber Pharmaceuticals, Inc. The label includes dosage strength, quantity of 100 tablets, and is marked Rx Only. It provides storage instructions and manufacturer details for Ascent Pharmaceuticals, Inc. and Camber Pharmaceuticals, Inc.*
FDA Label Image

20 Meq K- 100s Count (20 Meq K 100s)

20 Meq K- 100s Count (20 Meq K 100s)
Potassium Chloride Extended-Release Tablets, USP 1500 mg (20 mEq K) oral tablet label from Camber Pharmaceuticals, Inc. The label indicates a bottle containing 100 tablets, marked Rx only, with storage and handling instructions, dosage advisories, and manufacturer information including Ascent Pharmaceuticals, Inc. and Camber Pharmaceuticals, Inc.*

* 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.