Image 1
Chemical structure of Mexiletine Hydrochloride showing the aromatic ring with amino and methyl substituents, along with the hydrochloride component.*
Mexiletine Hydrochloride Capsule
Product Images NDC 0093-8739
4 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mexiletine Hydrochloride (NDC 0093-8739). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Teva Pharmaceuticals Usa, 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.
Image 2
Label for Mexiletine Hydrochloride Capsules USP 150 mg manufactured by Teva Pharmaceuticals USA, Inc. The label includes dosage form as capsules, packaging size of 100 capsules, and instructions to take with food or antacid. It also contains storage information, barcode, and manufacturer details.*
Image 3
Label for Mexiletine Hydrochloride Capsules USP 200 mg from Teva Pharmaceuticals USA, Inc. The label states the product is prescription only, includes directions to take with food or antacid, and specifies a package size of 100 capsules. Storage instructions and manufacturer details are also provided on the label.*
Image 4
Label for Mexiletine Hydrochloride Capsules USP 250 mg, a drug for further processing. The label includes usage instructions to take with food or antacid and indicates the package contains 100 capsules. The labeler is Teva Pharmaceuticals USA, Inc. Additional storage and safety information is included in smaller text.*
* 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.
