Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 0440-7605

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 0440-7605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Liberty Pharmaceuticals, 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

This Is An Image Of The Structural Formula Of Hydrocodone Bitartrate. (Hydrocodone Apap For Qualitest 1)

Chemical structure diagram showing the molecular structure of hydrocodone bitartrate dihydrate. The image includes the detailed atom and bond arrangement of the hydrocodone component and the additional bitartrate and water molecules, with molecular formula and weight noted.*

FDA Label Image

This Is An Image Of The Structural Formula Of Acetaminophen. (Hydrocodone Apap For Qualitest 2)

Chemical structure diagram showing two molecular formulas and structural formulas, representing the active ingredients of Hydrocodone Bitartrate and Acetaminophen. The diagram includes molecular formulas, structural bonds, and an indication of molecular weight (M.W. = 151.16) for one component.*

FDA Label Image

Image Label (Hydrocodone Apap For Qualitest 3)

Label for Hydrocodone Bitartrate and Acetaminophen tablets, generic for Norco, from Liberty Pharmaceuticals Inc. The dosage strength is 5 mg hydrocodone bitartrate and 325 mg acetaminophen per tablet. The package contains 10 tablets. The label includes prescription-only designation and dosing instructions with spaces for doctor and patient information. Manufactured for Qualitest Pharmaceuticals.*

* 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.