Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-0643

3 FDA label images from Redpharm Drug 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 67296-0643). 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.

Product Images & Figures Index

FDA Label Image

Copy Of Label (6729606433)

Copy Of Label (6729606433)
Label for Hydrocodone Bitartrate & Acetaminophen tablets, 7.5 mg / 500 mg strength, containing 15 tablets. The label includes prescription-only status, lot number 90110A 1, and expiration date 01/13. Manufactured for Qualitest Pharmaceuticals, Huntsville, AL, and distributed by RedPharm Drug, Eden Prairie, MN. The label also displays a barcode and a controlled substance schedule III symbol.*
FDA Label Image

Structural Formula (Image1)

Structural Formula (Image1)
Chemical structure diagram showing the molecular composition of hydrocodone bitartrate and acetaminophen, including the molecular formulas and molecular weight (494.5). The image depicts the spatial arrangement of atoms and bonds for these active ingredients.*
FDA Label Image

Structural Formula (Image2)

Structural Formula (Image2)
Chemical structure diagram showing the molecular formula C8H9NO2 and a structural formula with a molecular weight of 151.16. The diagram depicts a molecule with an acetyl group attached to an aromatic ring, consistent with acetaminophen's chemical structure.*

* 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.