Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 63629-2293

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 63629-2293). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure-1 (Hydrocodone Bitartrate And Acetaminophen Tablets 1)

Structure-1 (Hydrocodone Bitartrate And Acetaminophen Tablets 1)
Chemical structure diagram showing the molecular structures of hydrocodone bitartrate and acetaminophen. The image depicts the detailed atomic bonding and arrangement characteristic of these active ingredients.*
FDA Label Image

Structure-2 (Hydrocodone Bitartrate And Acetaminophen Tablets 2)

Structure-2 (Hydrocodone Bitartrate And Acetaminophen Tablets 2)
Chemical structure of Hydrocodone Bitartrate and Acetaminophen depicting the molecular arrangement including a hydroxyl group attached to a benzene ring and an acetamide functional group.*
FDA Label Image

Label (Lbl636292293)

Label (Lbl636292293)
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, strength 5 mg/325 mg, manufactured by Teks Pharma Inc. and relabeled by Bryant Ranch Prepack. The label includes storage instructions, dosage information, a barcode, and states the package contains 500 tablets with Rx only. The label highlights the active ingredients and dosage prominently.*

* 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.