Mexiletine Hydrochloride Capsule
Product Images NDC 50742-241

5 FDA label images from Ingenus Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mexiletine Hydrochloride (NDC 50742-241). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ingenus Pharmaceuticals, Llc, 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

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Chemical structure of Mexiletine hydrochloride, showing its molecular arrangement with a benzene ring substituted with amino, methoxypropyl, and methyl groups along with the hydrochloride component.*
FDA Label Image

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FDA Label Image

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Label for Mexiletine Hydrochloride Capsules USP 150 mg by Ingenus Pharmaceuticals, LLC. The label states the product contains 100 capsules and includes directions to take with food or antacid. Storage instructions and child-resistant container information are also visible, along with a barcode and NDC number 50742-239-01.*
FDA Label Image

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Label for Mexiletine Hydrochloride Capsules, USP 200 mg oral capsules by Ingenus Pharmaceuticals, LLC. The label indicates the package contains 100 capsules. It includes storage instructions, dosage advisory, a blue highlighted strength of 200 mg, and a barcode. The label also states 'Take with food or antacid' and is for prescription use only.*
FDA Label Image

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Packaging label for Mexiletine Hydrochloride Capsules, USP 250 mg by Ingenus Pharmaceuticals, LLC. The label indicates 100 capsules per container and includes directions to take with food or antacid. Storage and dispensing instructions, barcode, and manufacturer information are also present.*

* 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.