Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 71335-2118

3 FDA label images from Bryant Ranch Prepack · 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 71335-2118). 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.

Product Images & Figures Index

FDA Label Image

Hydrocodone Bitartrate- Struct (Structure 1)

Hydrocodone Bitartrate- Struct (Structure 1)
Chemical structure of Hydrocodone Bitartrate Dihydrate, showing the molecular formulas C18H21NO3 and C4H6O6 with 2 1⁄2 water molecules, and molecular weight 494.490.*
FDA Label Image

Acetaminophen- Struct (Structure 2)

Acetaminophen- Struct (Structure 2)
Chemical structure of acetaminophen showing its molecular formula C8H9NO2 and molecular weight 151.16. The diagram includes the arrangement of atoms and bonds in the acetaminophen molecule as depicted on the image.*
FDA Label Image

Label (Lbl713352118)

Label (Lbl713352118)
Label for Hydrocodone/Apap 10/325 mg tablet, a Schedule II controlled substance, packaged by Bryant Ranch Prepack. The label includes storage instructions (store at 20°-25°C), a caution about risk of overdose and addiction, and a warning that the drug may cause drowsiness. The label compares this product to Norco 10/325 mg by Ascent Pharmaceuticals, Inc. The tablet is described as a white oval marked T259. The package contains 20 tablets and features a barcode and NDC 71335-2118-1.*

* 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.