Methocarbamol Tablet
Product Images NDC 63187-087

View Photos of 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 Methocarbamol (NDC 63187-087). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

63187-019-45 (750mg30s)

63187-019-45 (750mg30s)
This is a description of a medication named Maracarbamal that contains Methocarbamol 750mg. It is packaged by Proficient Rx LP and comes in a container of 430 tablets. The tablets are white to off-white and capsule-shaped, with debossing of ‘H’ on one side and ‘115’ on the other side. The NDC code for Methocarbamol USP is 63187-019-30, and the product ID is PM001930. The medication should be stored at 20°-25°C (88°-77°F) and kept away from children. The expiration date is not available, but the lot number is 00000.*
FDA Label Image

63187-087-20 (Methocarbamol 500mg)

63187-087-20 (Methocarbamol 500mg)
This is a description of a drug product containing Methocarbamol 500 mg sold in a pack of 30 tablets. The package was produced by Proficient Rx LP and bears the NDC code 63187-087-30. The drug is only available by prescription, and the package information includes the drug name, dosage, lot number, and expiration date. The drug is stored at a temperature range of 20°C to 25°C and should be kept away from children. The GTIN code for the product is 00363187087302, and it was manufactured by Hetero Labs Limited in Hyderabad, India.*
FDA Label Image

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FDA Label Image

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* 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.