Methocarbamol Tablet, Coated
Product Images NDC 70518-1738

8 FDA label images from Remedyrepack Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Methocarbamol (NDC 70518-1738). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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 750mg 70518 1738 01

Methocarbamol 750mg 70518 1738 01
Label for Methocarbamol 750 mg coated tablets, quantity of 120. The label includes the proprietary and generic names, dosage strength, dosage form, and quantity. It states the product is RX only, includes the NDC 70518-1738-01, and repackaging information by RemedyRepack Inc., Indiana. The label also mentions the manufacturer as Granules India Ltd., Hyderabad, India, along with storage instructions and a barcode and QR code.*
FDA Label Image

Methocarbamol 750mg 70518 1738 02

Methocarbamol 750mg 70518 1738 02
Methocarbamol 750 mg coated tablets label showing a quantity of 100 tablets. The label indicates the product is prescription only, with the National Drug Code (NDC) 70518-1738-02 and repackaged by RemedyRepack Inc. Directions for use refer to the package insert. Storage instructions and manufacturer details (Granules India Ltd.) are included on the label.*
FDA Label Image

Methocarbamol 750mg 70518 1738 03

Methocarbamol 750mg 70518 1738 03
Methocarbamol 750 mg coated tablets packaging label showing quantity of 60 tablets. Label includes the product name, strength, dosage form, NDC number 70518-1738-03, and states it is for prescription use only. Manufacturer information lists Granules India Ltd., Hyderabad, India. The label advises to keep medication out of reach of children and refers to the package insert for directions. It also notes storage instructions and repackaging by RemedyRepack Inc.*
FDA Label Image

Methocarbamol 750mg 70518 1738 04

Methocarbamol 750mg 70518 1738 04
Label for Methocarbamol 750 mg coated tablets, quantity 30, by Remedy Repack Inc. The label includes the NDC number 70518-1738-04, manufacturer Granules India Ltd., and storage instructions with temperature ranges. It also notes directions for use are in the package insert and includes a barcode and QR code.*
FDA Label Image

Methocarbamol 750mg 70518 1738 05

Methocarbamol 750mg 70518 1738 05
Methocarbamol 750 mg coated tablets vial label with a quantity of 20 tablets. The label includes the NDC number 70518-1738-05, manufacturer details stating granules are from Granules India Ltd., Hyderabad, India, and repackaging information by RemedyRepack Inc. Directions advise to see package insert, storage temperature guidelines, and warnings to keep medication out of reach of children. The label features a purple and white color scheme with remedy repack logo.*
FDA Label Image

Methocarbamol 750mg 70518 1738 06

Methocarbamol 750mg 70518 1738 06
Label for Methocarbamol 750 mg coated tablets, containing 60 tablets per package. The drug is prescription-only and repackaged by RemedyRepack Inc. The label includes the NDC number 70518-1738-06, barcode, QR code, manufacturing information, and storage directions.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Methocarbamol 750 mg coated tablets label from RemedyRepack Inc. The label shows quantity of 30 tablets, NDC 70518-1738-00, with manufacturer listed as Granules India Ltd., Hyderabad, India. It includes storage instructions and a QR code on a white and purple background.*
FDA Label Image

Str (Metho)

Str (Metho)
Chemical structure diagram of methocarbamol, the active ingredient in Methocarbamol Tablets 750 mg by RemedyRepack Inc.*

* 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.