Methadone Hydrocloride Concentrate
Product Images NDC 0527-1927

3 FDA label images from Lannett Company, Inc. · 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Methadone Hydrochloride Oral Concentrate Usp Dye F 1)

Chemical Structure (Methadone Hydrochloride Oral Concentrate Usp Dye F 1)
Chemical structure of methadone hydrochloride showing the molecular formula C21H27NO with the hydrochloride component and a molecular weight of 345.91, depicted as a structural diagram with labeled atoms and molecular groups.*
FDA Label Image

30 mL Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 2)

30 mL Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 2)
Label of Methadone Hydrochloride dye-free, sugar-free, unflavored oral concentrate, USP, 10 mg/mL strength. The label states it contains 10 mg methadone hydrochloride per mL in a 30 mL bottle. It is indicated for oral use, Rx only, and distributed by Lannett Company, Inc. The label includes storage instructions, dosing guidelines, and a barcode with the product NDC 0527-1927.*
FDA Label Image

1 L Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 3)

1 L Bottle Label (Methadone Hydrochloride Oral Concentrate Usp Dye F 3)
Label for Methadone Hydrochloride Oral Concentrate USP dye-free, sugar-free, unflavored, 10 mg per mL, 1 Liter (1000 mL) bottle. The label includes a warning not to use if the seal around the bottle cap is broken or missing. Distributed by Lannett Company, Inc., Philadelphia, PA. Contains ingredients including citric acid anhydrous, purified water, and sodium benzoate.*

* 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.