Methocarbamol
Product Images NDC 61919-627

3 FDA label images from Directrx · 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 61919-627). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Directrx, 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

610 60

610 60
Packaging label for Methocarbamol 500 mg film-coated tablets, 60 count, labeled as generic for Robaxin. Manufactured for Canales Pharmaceuticals Inc. and packaged by DirectRx in Alpharetta, GA. Label includes warnings about alcohol and drowsiness, lot number, expiration date 04/20, and storage instructions to keep out of reach of children.*
FDA Label Image

903 90

903 90
METHOCARBAMOL 750 mg, bottle label for 90 tablets by DirectRX. The label notes it is a generic for Robaxin and each uncoated tablet contains Methocarbamol USP 750 mg. Includes NDC 61919-903-90 with lot number, expiration date 04/17, and cautionary storage instructions. Multiple panel repeats display dosage info and warnings about drowsiness and alcohol use.*
FDA Label Image

Label (Methocarb627)

Label (Methocarb627)
METHOCARBAMOL 750mg 90 Tablets label for a product distributed by DirectRX. The label indicates the product is a generic for Robaxin, with each tablet containing 750 mg of Methocarbamol. The label includes lot number, expiration date (04/17), and packaging details. It also features warnings about drowsiness, alcohol interaction, and storage instructions, with the NDC number 61919-627-90.*

* 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.