Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 71335-2585

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 71335-2585). 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 two separate molecules. The left structure depicts a complex fused ring system with nitrogen and oxygen atoms, characteristic of hydrocodone. The right structure shows a simpler molecule with two carboxylic acid groups and hydroxyl groups, labeled with 1/2 H2O, representing the hydrate form of acetaminophen or a related compound.*
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, showing molecular bonds and arrangement of atoms including hydroxyl and acetyl functional groups.*
FDA Label Image

Label (Lbl713352585)

Label (Lbl713352585)
Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg/325 mg, oral tablets. The package contains 30 tablets, repackaged by Bryant Ranch Prepack, Inc., and manufactured by Tris Pharma, Inc. The label includes storage instructions, caution warnings, and dosing reference with QR codes for full prescribing information.*

* 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.