Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 63739-455

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 63739-455). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mckesson Packaging Services Business Unit Of Mckesson Corporation, 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

Hydrocodone Bitartrate Structural Formula (084efc66 F1e9 4000 8694 E251b41b5991 01)

Hydrocodone Bitartrate Structural Formula (084efc66 F1e9 4000 8694 E251b41b5991 01)
Chemical structure diagram of Hydrocodone Bitartrate, showing molecular components including C18H21NO3 and C4H6O6 with 2.5 H2O. The molecular weight is 494.490.*
FDA Label Image

Acetaminophen Structural Formula (084efc66 F1e9 4000 8694 E251b41b5991 02)

Acetaminophen Structural Formula (084efc66 F1e9 4000 8694 E251b41b5991 02)
Chemical structure of acetaminophen showing its molecular formula as C8H9NO2 and molecular weight of 151.16.*
FDA Label Image

Hydrocodone And Acetaminophen Label (084efc66 F1e9 4000 8694 E251b41b5991 03)

Hydrocodone And Acetaminophen Label (084efc66 F1e9 4000 8694 E251b41b5991 03)
The image displays a drug label for HYDROCODONE BITARTRATE AND ACETAMINOPHEN 5 mg / 500 mg Tablets, USP. It shows the NDC number 63739-455-10 and indicates a package of 100 tablets (10x10). The label includes the logo for SKY and provides some usage and storage instructions. The labeler is McKesson Packaging Services Business Unit of McKesson Corporation.*

* 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.