Methadone Hydrochloride
Product Images NDC 17856-3553

3 FDA label images from Atlantic Biologicals Corp. · 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 17856-3553). 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.

Product Images & Figures Index

FDA Label Image

Label 1 (17856 3553 01 Label)

Label 1 (17856 3553 01 Label)
Methadone Hydrochloride Intensol oral concentrate, 10 mg per 1 mL, in a unit dose delivering 1 mL oral syringe. The label includes packaging information with dosage per syringe (1 mL) and case quantity (60 syringes). It is labeled as Rx only, repackaged by Unit Dose Solutions, and distributed by Atlantic Biologicals Corp. Storage instructions and a barcode are also visible.*
FDA Label Image

Label 2 (17856 3553 02 Label)

Label 2 (17856 3553 02 Label)
Text panel for Methadone Hydrochloride Intenso Oral Concentrate USP 5 mg per 0.5 mL shows dosage per syringe, storage instructions, safety warnings to keep out of reach of children, repackager and distributor information from Atlantic Biologics Corp., and contact information including a phone number. It includes lot number, manufacturing lot, expiration date fields, and a barcode.*
FDA Label Image

Dolophine.bmp (Image 01)

Dolophine.bmp (Image 01)
Chemical structure of Methadone Hydrochloride showing its molecular framework with carbon, hydrogen, nitrogen, and oxygen atoms clearly illustrated along with the hydrochloride (HCl) component.*

* 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.