Methadone Hydrocloride
Product Images NDC 17856-1928

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 17856-1928). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Label 1 (17856 1928 03)

Label 1 (17856 1928 03)
Label for Methadone Hydrochloride oral concentrate, USP, delivering 2.5 mg per 0.25 mL dose. The product is sugar-free, dye-free, and unflavored. Packaging indicates it contains 60 syringes and is distributed by Atlantic Biologicals Corp. Storage instructions note controlled room temperature of 20 to 25°C (68 to 77°F).*
FDA Label Image

Label 2 (17856 1928 05)

Label 2 (17856 1928 05)
Label for Methadone Hydrochloride oral concentrate USP delivering 5 mg per 0.5 mL in a dosage of 5 syringes. The product is sugar-free, dye-free, and unflavored. Labeled by Atlantic Biologicals Corp, with storage instructions at controlled room temperature (20° to 25°C). The label includes a barcode, GTIN, serial number, expiration date, lot number, and a DEA Schedule II classification.*
FDA Label Image

Structural Formula (Methadone Hydrochloride Oral Concentrate Usp Dye F 1)

Structural Formula (Methadone Hydrochloride Oral Concentrate Usp Dye F 1)
Chemical structure diagram of Methadone Hydrochloride showing its molecular formula C21H27NO and molecular weight of 345.91. The structure includes labeled functional groups and the HCl component indicating the hydrochloride salt form.*

* 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.