Structural Formula (Methadone Hydrochloride Injection Usp 1)
Methadone Hydrochloride Injection
Product Images NDC 0641-6266
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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.
Methadone Vial Label (Methadone Hydrochloride Injection Usp 2)
This is a description of a prescription drug - Methadone Hydrochloride Injection, containing 200 mg per 20 mL (10 mg per mL). It is intended for intravenous, intramuscular, or subcutaneous use in multiple doses. The formulation includes 10 mg of methadone hydrochloride per mL and various inactive ingredients. The solution has a pH between 3.0 to 6.5 and should be stored within a temperature range of 15-30°C. Manufacturer details indicate it is made by Hikma in Berkeley Heights, NJ. For specific dosage instructions, refer to the accompanying prescribing information.*
Carton (Methadone Hydrochloride Injection Usp 3)
This is a description for a prescription medication called Methadone Hydrochloride Injection, USP. It contains 200 mg per 20 mL (10 mg per mL) for intravenous, intramuscular, or subcutaneous use. Each vial contains 10 mg of methadone hydrochloride equivalent to 8.95 mg of methadone base. The storage instructions are to keep the medication between 15°C-30°C (59°F-86°F) and protect it from light. Additional dosage information should be obtained from the prescribing information.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
