Methocarbamol Tablet, Film Coated
Product Images NDC 0615-8506

View Photos of 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 Methocarbamol (NDC 0615-8506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ncs Healthcare Of Ky, Llc Dba Vangard Labs, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Methocarbamol 8506 8507 1)

Chemical Structure (Methocarbamol 8506 8507 1)
Chemical structure diagram of methocarbamol illustrating its molecular framework with a benzene ring, hydroxyl group, methoxy group, and carbamate functional group.*
FDA Label Image

Principal Display Panel (Methocarbamol 8506 8507 2)

Principal Display Panel (Methocarbamol 8506 8507 2)
Methocarbamol Tablets USP 500 mg film-coated tablets labeling from NCS HealthCare of KY, LLC dba Vangard Labs. The label indicates the quantity of 30 tablets, with manufacturing by Aurobindo and packaging by Vangard in Glasgow, KY. Multiple barcode labels and storage instructions are displayed, along with an institutional use notice.*
FDA Label Image

Principal Display Panel (Methocarbamol 8506 8507 3)

Principal Display Panel (Methocarbamol 8506 8507 3)
Label for Methocarbamol Tablets USP 750 mg film coated oral tablets. Manufactured by Aurobindo and packaged by Vangard Labs, Glasgow, KY. The label displays quantity as 30 tablets and includes multiple barcode sections with lot number and storage instructions to keep between 20°-25°C. Marked for institutional use only.*

* 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.