Hycodan
Product Images NDC 64950-205

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hycodan (NDC 64950-205). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genus Lifesciences 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.

FDA Label Image

Chemical Structure (Hycodan 01)

Chemical structure diagram of the active ingredient in Hycodan by Genus Lifesciences Inc., depicting a complex molecule with multiple rings, hydroxyl groups, a methoxy group, and associated acidic components with water molecules indicated.*

FDA Label Image

Chemical Structure (Hycodan 02)

Chemical structure diagram of the active ingredient in Hycodan, showing its molecular framework with a phenyl group and other chemical bonds, along with a methyl bromide (Me Br) component.*

FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Label for Hycodan tablets containing hydrocodone bitartrate 5 mg and homatropine methylbromide 1.5 mg. The label indicates a 30-tablet count and includes the NDC 64950-205-03. Manufactured by Genus Lifesciences Inc., Allentown, PA, it features storage instructions and a child-resistant container warning. The label also shows a barcode and the statement "NO VARNISH."*

FDA Label Image

Hycodan 04

Label for Hycodan oral solution containing hydrocodone bitartrate 5 mg and homatropine methylbromide 1.5 mg per 5 mL. The 473 mL bottle is manufactured by Genus Lifesciences Inc. The label includes dosage information, storage instructions at 25°C, and a note to dispense the Medication Guide with the product. NDC 64950-342-47 is visible with a barcode and GTIN.*

* 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.