Hydrocodone Bitartrate And Homatropine Methylbromide Solution
Product Images NDC 64950-371

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Homatropine Methylbromide (NDC 64950-371). 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 (Hydrocodone 01)

Chemical structure diagram showing the active ingredients hydrocodone bitartrate and homatropine methylbromide, including associated molecules and water of hydration, represented by structural formulas and chemical notation.*

FDA Label Image

Chemical Structure (Hydrocodone 02)

Chemical structure diagram of Hydrocodone Bitartrate and Homatropine Methylbromide showing molecular bonds and arrangement of atoms for this active ingredient combination.*

FDA Label Image

Principal Display Panel (30 Tablet Bottle Label)

Label for Hydrocodone Bitartrate and Homatropine Methylbromide Tablets, 5 mg / 1.5 mg strength. The label includes dosage details, storage instructions, and manufacturer information for Genus Lifesciences Inc., Allentown, PA. It indicates a package of 30 tablets and displays the NDC 64950-206-03 and a barcode.*

FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Label for Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution with a strength of 5 mg/1.5 mg per 5 mL. The solution is manufactured by Genus Lifesciences Inc. in Allentown, PA, and comes in a 473 mL bottle. The label includes dosage instructions, storage conditions, and a barcode.*

* 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.