Chemical Structure (Methadone Hydrochloride Oral Concentrate Usp Dye F 1)
Methadone Hydrocloride Concentrate
Product Images NDC 0527-1927
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 Hydrocloride (NDC 0527-1927). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lannett Company, 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.
30 mL Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 2)
1 L Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 3)
This is a description for Methadone Hydrochloride Oral Concentrate, USP provided by Lannett Company, Inc. The concentrate is dye-free, sugar-free, and unflavored. Each milliliter contains Methadone Hydrochloride, USP, and other ingredients such as Purified Water, Sodium Benzoate, and Giric Add Anhydrous. The usual dosage is to be determined by the physician and to be diluted with at least 30 mL of water or other liquid before oral administration. The concentrate should be preserved in light containers, protected from light, and stored at room temperature between 20°C to 25°C (68°F to 77°F). The bottle seal must not be broken or missing. The product is packaged in 1-liter (1000 mL) bottles with NoC 0527-1927-39.*
* 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.
