Hydrocodone Bitartrate And Acetaminophen Solution
Product Images NDC 60687-417

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 60687-417). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Cup

Label for Hydrocodone Bitartrate and Acetaminophen oral solution by American Health Packaging. The product strength is 7.5 mg/325 mg per 15 mL with 7% alcohol content. The label includes the NDC 60687-417-44, a barcode, and indications for prescription use and institutional use only.*

FDA Label Image

Tray

A drug facts or instruction panel for Hydrocodone Bitartrate and Acetaminophen Oral Solution. It includes usage restrictions such as 'Rx Only' and 'For Institutional Use Only,' pharmacist dispensing instructions, storage temperature guidelines, a child safety warning, and a note stating that a DEA order form is required.*

FDA Label Image

Acetaminophen Structure (Hycod Str)

Chemical structure diagram of Hydrocodone Bitartrate and Acetaminophen showing the acetaminophen molecule with its characteristic benzene ring, hydroxyl group, and amide functional group.*

FDA Label Image

Hydrocodone Bitartrate Structure (Hydcod Structure)

Chemical structure diagram showing the molecular formula of Hydrocodone Bitartrate, including the bifurcated ring system and associated functional groups, along with the molecular structure of tartaric acid and 2.5 molecules of water (2 1/2 H2O) indicating the hydrate form.*

* 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.