Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 71335-1417

3 FDA label images from Bryant Ranch Prepack · 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 Hydrocodone Bitartrate And Acetaminophen (NDC 71335-1417). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Hydrocodone 01)
Chemical structure diagram showing two molecules: hydrocodone bitartrate on the left and acetaminophen on the right, including its associated hydrate (2.5 water molecules). The illustration depicts atom connectivity and chemical groups relevant to the active ingredients in the Hydrocodone Bitartrate and Acetaminophen oral tablet.*
FDA Label Image

Chemical Structure (Hydrocodone 02)

Chemical Structure (Hydrocodone 02)
Chemical structure diagram showing a molecule with a benzene ring bonded to a hydroxyl group (OH) on one side and an acetamide group (CH3CONH) on the other. This corresponds to the chemical structure of acetaminophen.*
FDA Label Image

Label Image (Lbl713351417)

Label Image (Lbl713351417)
Label for Hydrocodone Bitartrate and Acetaminophen 5 mg/325 mg oral tablet, packaged by Bryant Ranch Prepack. The label includes dosing strength, a comparison to Norco 5/325 mg, controlled substance classification (CII), and storage instructions at 20°-25°C (68°-77°F). It also shows a caution for risk of overdose and addiction, a lot number, an NDC number 71335-1417, 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.