Mexiletine Hydrochloride
Product Images NDC 10135-731

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mexiletine Hydrochloride (NDC 10135-731). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex 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.

FDA Label Image

Mhc-150 (Mhc 150)

Label for Mexiletine Hydrochloride Capsules, USP 150 mg, manufactured by Marlex Pharmaceuticals, Inc. The label indicates the product contains 100 capsules, prescription use only, and advises taking with food or antacid. Storage instructions specify 25°C with allowed excursions, and it includes a child-resistant closure warning.*

FDA Label Image

Mhc-200 (Mhc 200)

Label for Mexiletine Hydrochloride Capsules, USP 200 mg by Marlex Pharmaceuticals, Inc. The label states to take with food or antacid and indicates the package contains 100 capsules. Storage instructions, dosage note, child-resistant closure mention, and manufacturer details are included alongside a barcode and NDC number 10135-0731-01.*

FDA Label Image

Mhc-250 (Mhc 250)

The packaging label for Mexiletine Hydrochloride Capsules, USP 250 mg by Marlex Pharmaceuticals, Inc. It shows product name, strength (250 mg), capsule form, and quantity (100 capsules). The label includes usage instructions, storage conditions, manufacturer details, and a barcode.*

FDA Label Image

Structure (Structure)

Chemical structure of Mexiletine Hydrochloride, showing a benzene ring substituted with methyl groups, an ether linkage to an aminoethyl side chain, and a hydrochloride (HCl) salt form.*

* 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.