Methadone Hydrochloride Concentrate
Product Images NDC 17856-0392

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 17856-0392). 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

Image 1 (17856 0392 1)

Image 1 (17856 0392 1)
This is a prescription drug called Methadone HCl Oral Concentrate USP (Cherry) with a dosage of 0.5mg/0.5ml and packaged by Unit Dose Solutions. It is distributed by Atlantic Biologicals and comes with a syringe for administering. The lot number is 000000 and it has an expiration date of 11714119. The drug is stored at a temperature between 0-77°F, and excursions are permitted from 10-85°F. The text includes other numbers and codes related to packaging and distribution, but there is no further useful information available.*
FDA Label Image

Image 2 (17856 0392 2)

Image 2 (17856 0392 2)
This is a description of a medication called Methadone Hydrochloride, which is an oral concentrate available in a USP 10mg per mL oral syringe. The package comes with a total of 60 syringes, containing cherry-flavored concentrate. The distribution company is Atlantic Biologicals and the medication is manufactured by the West-Ward. The lot number and expiration date is provided on the package for safety purposes. There are instructions for dosing and administration, and there is a phone number provided for reordering.*
FDA Label Image

Chemical Structural (Chem)

* 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.