Methadone Hydrochloride Injection
Product Images NDC 0641-6266

View Photos of 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 Methadone Hydrochloride (NDC 0641-6266). 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 (Methadone Hydrochloride Injection Usp 1)

Structural Formula (Methadone Hydrochloride Injection Usp 1)
Chemical structure of Methadone Hydrochloride showing the molecular arrangement with two benzene rings and associated groups, consistent with the active ingredient methadone hydrochloride.*
FDA Label Image

Methadone Vial Label (Methadone Hydrochloride Injection Usp 2)

Methadone Vial Label (Methadone Hydrochloride Injection Usp 2)
Label for Methadone Hydrochloride Injection, USP, 10 mg/mL (200 mg per 20 mL) multiple-dose vial. Intended for intravenous, intramuscular, or subcutaneous use. Manufactured by Hikma Pharmaceuticals USA Inc. Contains product usage, storage instructions, and inactive ingredients.*
FDA Label Image

Carton (Methadone Hydrochloride Injection Usp 3)

Carton (Methadone Hydrochloride Injection Usp 3)
Methadone Hydrochloride Injection, USP 10 mg/mL vial label for 200 mg per 20 mL solution by Hikma Pharmaceuticals USA Inc. The label shows dosage form as injection, for intravenous, intramuscular, or subcutaneous use. Includes NDC 0641-6266-01 and storage instructions, active and inactive ingredient details, dosage and handling 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.