Methocarbamol
Product Images NDC 65977-5033

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Methocarbamol (NDC 65977-5033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hetero Drugs Limited Unit Iii, 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

Iamges (Methocarbamol Tablet Figure 1)

Chemical structure of Methocarbamol, depicting its molecular formula with aromatic ring, hydroxyl, methoxy, and carbamate functional groups.*

FDA Label Image

750mg100 (Methocarbamol Tablet Figure 10)

Methocarbamol Tablets USP 750 mg packaging label displaying a 100-count bottle. The label includes dosage information for adults, storage instructions, and the product's NDC. The manufacturer is Hetero Drugs Limited Unit III, Hyderabad, India. The label features a barcode and directs dispensing in a tight container.*

FDA Label Image

750mg500 (Methocarbamol Tablet Figure 11)

Methocarbamol Tablets USP 750 mg label showing product name and strength prominently in green and white. The label indicates the quantity is 500 tablets and that the product is for prescription use only. Manufacturer details read Hetero Drugs Limited Unit III, with storage instructions and dosage directions also visible.*

FDA Label Image

Xcvxcv (Methocarbamol Tablet Figure 2)

FDA Label Image

30tablets (Methocarbamol Tablet Figure 3)

Methocarbamol Tablets USP 500 mg packaging label showing a white and light blue color scheme. The label indicates the product contains 30 tablets and is manufactured by Hetero Drugs Limited Unit III. The label includes usage instructions advising typical dosing and storage information on temperature and light exposure.*

FDA Label Image

500mg60 (Methocarbamol Tablet Figure 4)

Methocarbamol Tablets USP 500 mg carton label displaying the product name, strength, and dosage form. The label indicates a package of 60 tablets, states 'Rx only', and includes directions for use and storage. The manufacturer is Hetero Drugs Limited Unit III. The label also shows a barcode and various regulatory information.*

FDA Label Image

500mg100 (Methocarbamol Tablet Figure 5)

Methocarbamol Tablets USP 500 mg bottle label with 100 tablets by Hetero Drugs Limited Unit III. Label includes USUAL DOSAGE instructions to take two tablets four times daily and storage conditions at 20° to 25°C (68° to 77°F). Contains barcode and lot information area.*

FDA Label Image

500mg500 (Methocarbamol Tablet Figure 6)

Methocarbamol Tablets USP 500 mg packaging label from Hetero Drugs Limited Unit III. The label shows the product name, strength of 500 mg, and indicates a count of 500 tablets. It includes storage instructions and a barcode. The product NDC number is 65977-5033-3.*

FDA Label Image

500mg1000tab (Methocarbamol Tablet Figure 7)

Methocarbamol Tablets USP 500 mg bottle label showing the product name and strength prominently. The label indicates the package contains 1000 tablets, with usual dosage and storage instructions. Manufactured by Hetero Drugs Limited Unit III in India, it also includes an NDC number and a barcode.*

FDA Label Image

750mg30 (Methocarbamol Tablet Figure 8)

Methocarbamol Tablets USP 750 mg packaging label displays the product name and strength prominently in green and blue text. The label indicates a quantity of 30 tablets, prescription only. The labeler is Hetero Drugs Limited Unit III. The label includes an NDC number, barcode, and storage instructions.*

FDA Label Image

750mg60tab (Methocarbamol Tablet Figure 9)

Methocarbamol Tablets USP 750 mg package label showing 60 tablets. The label includes a barcode, dosage storage instructions, and is labeled for prescription use only. Manufactured by Hetero Drugs Limited Unit III, Hyderabad, India.*

* 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.