Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 66336-012

View Photos of 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 66336-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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

Ndc 66336-0012-xx (Ndc 66336 0012 Xx Qualitest)

Ndc 66336-0012-xx (Ndc 66336 0012 Xx       Qualitest)
Label for Hydrocodone Bitartrate And Acetaminophen tablets, each containing 7.5 mg hydrocodone bitartrate and 500 mg acetaminophen. The label shows the NDC 66336-0012-XX, indicates the product is RX only, and includes warnings about habit formation and driving impairment. The label also displays Dispensing Solutions, Inc. as the packager and features storage instructions and dosage guidance.*
FDA Label Image

This Is An Image Of The Structural Formula Of Hydrocodone Bitartrate. (Hydro 1)

This Is An Image Of The Structural Formula Of Hydrocodone Bitartrate. (Hydro 1)
Chemical structure diagram representing Hydrocodone Bitartrate and Acetaminophen, including molecular formulas, structural bonds, and water molecule components, with a molecular weight noted as 494.5.*
FDA Label Image

This Is An Image Of The Structural Formula Of Acetaminophen. (Hydro 2)

This Is An Image Of The Structural Formula Of Acetaminophen. (Hydro 2)
Chemical structure diagram showing the molecular composition of the active ingredient related to Hydrocodone Bitartrate and Acetaminophen, including labeled atoms and molecular weight (M.W. = 151.16).*

* 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.