Mexiletine Hydrochloride
Product Images NDC 0527-4109

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mexiletine Hydrochloride (NDC 0527-4109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

150mg Bottle Label (150 mg Bottle Label)

Label of Mexiletine Hydrochloride Capsules, USP 150 mg by Lannett Company, Inc. The label indicates a prescription product with 100 capsules per package. It includes storage instructions, dosage form, and safety warnings about child-resistant dispensing and medication storage out of children's reach.*

FDA Label Image

200mg Bottle Label (200 mg Bottle Label)

Label for Mexiletine Hydrochloride Capsules, USP 200 mg by Lannett Company, Inc. The label indicates 100 capsules per bottle and includes storage instructions to keep at 25°C with permitted excursions. It notes the capsules contain 200 mg mexiletine hydrochloride each and advises to take with food or antacid. The label also displays barcode, NDC 05274-1083, and warnings to keep out of reach of children.*

FDA Label Image

250mg Bottle Label (250 mg Bottle Label)

Mexiletine Hydrochloride Capsules, USP 250 mg label from Lannett Company, Inc. The label states 100 capsules per package, with drug information and storage instructions. It includes manufacturer and distributor details, a barcode, and cautionary notes regarding medication use and child-resistant closure.*

FDA Label Image

Chemical Structure (Mexiletine 01)

Chemical structure diagram of Mexiletine Hydrochloride, showing molecular bonds and functional groups characteristic of this active ingredient.*

* 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.