Robaxin Injection
Product Images NDC 0641-6217

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Robaxin (NDC 0641-6217). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Robaxin Injectable Novaplus 1)

Chemical structure diagram of methocarbamol, the active ingredient in ROBAXIN injection 100 mg/mL by Hikma Pharmaceuticals USA Inc. The structure shows the molecular arrangement including aromatic rings, oxygen, nitrogen, and hydroxyl groups.*

FDA Label Image

462-766-00 (Robaxin Injectable Novaplus 2)

Label for ROBAXIN Injectable methocarbamol injection, USP, with a strength of 1,000 mg per 10 mL (100 mg/mL). The label indicates a 10 mL single-dose vial for intramuscular or intravenous use. Manufactured by West-Ward, a division of Hikma Pharmaceuticals USA Inc., located in Eatontown, NJ. The label includes the product NDC 0641-6217-01 and regulatory text.*

FDA Label Image

462-767-00 (Robaxin Injectable Novaplus 3)

Label for ROBAXIN Injectable (Methocarbamol Injection, USP) 100 mg/mL in 10 mL single-dose vials. Contains 1,000 mg/10 mL strength packaged as 25 vials. Suitable for intravenous or intramuscular injection. Manufactured by West-Ward, Eatontown, NJ. Includes storage directions and dosage form details.*

FDA Label Image

Robaxin Injectable Novaplus 4

The image shows a label on a vial of ROBAXIN (methocarbamol) injection, 100 mg/mL, by Hikma Pharmaceuticals USA Inc. The label includes a QR code and placeholders for GTIN, serial number (SN), expiration date (EXP), and lot number (LOT) information.*

* 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.