Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 68071-4853

3 FDA label images from Nucare Pharmaceuticals,inc. · 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 68071-4853). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

Pdp (68071 4853 2)

Pdp (68071 4853 2)
Label for Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablets by NuCare Pharmaceuticals, Inc. The label shows the quantity of 20 tablets, identifies the product as prescription only (Rx Only), and includes dosage form as tablets. The label lists manufacturer AuroLife Pharma LLC and packager Orange Pharmaceuticals, with instructions to keep out of reach of children and store at controlled temperature 68-77°F. Additional regulatory and tracking information such as NDC numbers, lot, expiration, and warnings about habit forming are also present.*
FDA Label Image

Chemical Structure (Hydrocodone Str1)

Chemical Structure (Hydrocodone Str1)
Chemical structure diagram of Hydrocodone Bitartrate and Acetaminophen, showing molecular arrangement with accompanying molecular formula C18H21NO3•C4H6O6•2½H2O and molecular weight 494.49.*
FDA Label Image

Chemical Structure (Hydrocodone Str2)

Chemical Structure (Hydrocodone Str2)
Chemical structure of acetaminophen, showing its molecular formula C8H9NO2 and molecular weight 151.16. The diagram includes the phenol and amide functional groups.*

* 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.