Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 52959-735

3 FDA label images from H.j. Harkins Company, 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 52959-735). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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.

Product Images & Figures Index

FDA Label Image

Label (52959 0735 Ppac Label)

Label (52959 0735 Ppac Label)
Label for HYDROCODONE BITARTRATE AND ACETAMINOPHEN 7.5/325 mg tablets, supplied by H.J. Harkins Company, Inc. The label includes cautionary federal law text prohibiting unauthorized transfer and dispensing. Product details show NDC 52959-0735-XX, with lot number, expiration date, and manufacturer AUROBINDO info. Multiple small boxes on the right repeat product name, NDC, lot, expiration, and quantity fields. The label also states 'Use As Directed by Physician' and includes a repack address in Grover Beach, CA.*
FDA Label Image

Image 1 (Image 1)

Image 1 (Image 1)
Chemical structure of acetaminophen (paracetamol) showing the molecular formula C8H9NO2 and molecular weight 151.16. The structure includes a benzene ring with hydroxyl and amide functional groups attached.*
FDA Label Image

Image (Image)

Image (Image)
Chemical structure of hydrocodone bitartrate with molecular formula C18H21NO3·C4H6O6·2½H2O and molecular weight 494.49, showing structural representation of the active ingredient in hydrogen and oxygen arrangement.*

* 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.