Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-0589

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 67296-0589). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Copy Of Label (6729605891)

Copy Of Label (6729605891)
Packaged label of Hydrocodone Bitartrate and Acetaminophen tablets, strength 7.5/325 mg. The label shows a quantity of 30 tablets and indicates that it is a prescription-only medication. Manufactured by Qualitest Pharmaceuticals in Huntsville, AL, and distributed by Redpharm Drug in Eden Prairie, MN. Label includes lot number 48H09A1 and expiration date 11/11. The label features a barcode and the schedule III controlled substance symbol.*
FDA Label Image

Structural Formula (Image1)

Structural Formula (Image1)
Chemical structure diagram showing the molecular formula and hydrated form of hydrocodone bitartrate, along with the molecular weight (494.5). The structure includes detailed bond lines and functional groups illustrating the compound.*
FDA Label Image

Structural Formula (Image2)

Structural Formula (Image2)
Chemical structure diagram showing a molecular formula with elements C8H9NO2 and a molecular weight of 151.16, related to the active ingredient in HYDROCODONE BITARTRATE AND ACETAMINOPHEN by RedPharm Drug Inc.*

* 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.