Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 42254-340

4 FDA label images from Rebel Distributors Corp · Packaging, Regulatory Labels, and Product Appearance

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 42254-340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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-structure (A46da71a 5fe1 4021 B866 4a806a12efa8 01)

Hydrocodone-structure (A46da71a 5fe1 4021 B866 4a806a12efa8 01)
Chemical structure diagram showing the molecular structures of hydrocodone bitartrate and its associated components, including the bitartrate salt and water of hydration, relevant to the drug hydrocodone bitartrate and acetaminophen.*
FDA Label Image

Acetaminophen-structure (A46da71a 5fe1 4021 B866 4a806a12efa8 02)

Acetaminophen-structure (A46da71a 5fe1 4021 B866 4a806a12efa8 02)
Chemical structure of acetaminophen shown as a molecular diagram with atoms and bonds indicating its chemical composition.*
FDA Label Image

Dea (A46da71a 5fe1 4021 B866 4a806a12efa8 03)

FDA Label Image

Hydrocodone 5mg/acet 325mg (A46da71a 5fe1 4021 B866 4a806a12efa8 04)

Hydrocodone 5mg/acet 325mg (A46da71a 5fe1 4021 B866 4a806a12efa8 04)
Label for Hydrocodone 5 mg and Acetaminophen 325 mg tablets, quantity 90, manufactured by Sun Pharmaceutical Industries, Inc. The label includes product identification, dosage information, and storage instructions. It is branded under Physician Partner, a division of Rebel Distributors Corp, with NDC 42254-340-90.*

* 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.