Potassium Chloride
Product Images NDC 67296-1771

3 FDA label images from Redpharm Drug, 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 67296-1771). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Label (67296 1771)

Label (67296 1771)
Label for Potassium Chloride ER 10 mEq (750 mg) extended-release tablets, 30 count. The label includes NDC 67296-1771-3 and states Rx Only. Manufacturer is Strides Shasun Ltd, India, and distributed by RedPharm Drug, Inc., Eden Prairie, MN.*
FDA Label Image

600mg (853af0b0 Dc2a 46ce 9ca2 89dc07cae63d 01)

600mg (853af0b0 Dc2a 46ce 9ca2 89dc07cae63d 01)
Potassium Chloride Extended-Release Tablets, USP, 8 mEq (600 mg) strength, in a 100-tablet package. The label includes dosage guidance, storage instructions, and manufacturer information for Strides Pharma Science Limited and distributor Strides Pharma Inc. The label also features barcodes and a warning to keep out of reach of children.*
FDA Label Image

750mg (853af0b0 Dc2a 46ce 9ca2 89dc07cae63d 02)

750mg (853af0b0 Dc2a 46ce 9ca2 89dc07cae63d 02)
Label for Potassium Chloride Extended-Release Tablets, USP 10 mEq (750 mg) by Strides Pharma Inc. The label states each tablet contains 750 mg Potassium Chloride USP. The package contains 100 tablets and is Rx only. Manufacturer is Strides Pharma Science Limited, India, distributed by Strides Pharma Inc., East Brunswick, NJ. Storage and usage instructions and warning to keep out of reach of children are also included.*

* 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.