Methocarbamol Tablet, Coated
Product Images NDC 70010-770

3 FDA label images from Granules Pharmaceuticals Inc. · 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 70010-770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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

Methocarbamol-structure (Methocarbamol Structure)

Methocarbamol-structure (Methocarbamol Structure)
Chemical structure of Methocarbamol, the active ingredient in Methocarbamol Tablets. The diagram shows the molecular arrangement including aromatic rings, hydroxyl, carbamate, and methoxy functional groups.*
FDA Label Image

Methocarbamol-500mg-100s (Methocarbamol 500mg 100s)

Methocarbamol-500mg-100s (Methocarbamol 500mg 100s)
Label for Methocarbamol Tablets, USP 500 mg oral film-coated tablets. The label indicates a count of 100 tablets with NDC 70010-754-01. Manufactured by Granules Pharmaceuticals Inc. in Chantilly, VA, and Granules India Limited in Hyderabad, India. The label includes storage instructions, a barcode, and a designated varnish area for batch coding.*
FDA Label Image

Methocarbamol-750mg-100s (Methocarbamol 750mg 100s)

Methocarbamol-750mg-100s (Methocarbamol 750mg 100s)
Packaging label for Methocarbamol Tablets USP, 750 mg, coated oral tablets. The label states the product contains 100 tablets, is manufactured by Granules India Limited, and labeled by Granules Pharmaceuticals Inc. It includes storage instructions, barcode, and a batch coding area with a 2D barcode. The label is predominantly white with purple accents.*

* 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.