Hydrocodone Bitartrate And Ibuprofen
Product Images NDC 54868-4976

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Ibuprofen (NDC 54868-4976). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Hydrocodone Bitartrate Structural Formula (Hydrocodone Bitartrate And Ibuprofen Tablets 7 5 M 1)

Chemical structure of hydrocodone bitartrate shown as a detailed two-dimensional molecular diagram with associated functional groups and water of hydration.*

FDA Label Image

Ibuprofen Structural Formula (Hydrocodone Bitartrate And Ibuprofen Tablets 7 5 M 2)

Chemical structure diagram of the active ingredient in HYDROCODONE BITARTRATE AND IBUPROFEN, displaying molecular bonds, carbon ring, and functional groups.*

FDA Label Image

Company Logo (Hydrocodone Bitartrate And Ibuprofen Tablets 7 5 M 3)

HYDROCODONE BITARTRATE AND IBUPROFEN in blister packaging. The product is a combination of hydrocodone bitartrate and ibuprofen tablets. The packaging is silver foil with individual compartments for each tablet. The labeler is Physicians Total Care, Inc. The NDC is 54868-4976.*

FDA Label Image

Image Of Package Label (Package Label)

Packaged label for HYDROCODONE BITARTRATE AND IBUPROFEN 7.5 mg / 200 mg tablets by Physicians Total Care, Inc. The label shows the quantity as 30 tablets and includes usage, storage, and caution information, with a NDC number 54868-4976-75. It displays barcodes, lot number, and expiration date details.*

* 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.