Acetaminophen And Codeine Phosphate Tablet
Product Images NDC 68071-3824

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 Acetaminophen And Codeine Phosphate (NDC 68071-3824). 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 3824 6)

Pdp (68071 3824 6)
Acetaminophen and Codeine Phosphate 300 mg / 30 mg oral tablets label from NuCare Pharmaceuticals, Inc. The label specifies a round, flat-faced, beveled edge, white, scored tablet with markings '2064' and 'V' on one side and '3' on the reverse. It includes dosage details for Acetaminophen and Codeine Phosphate, product number P07590066ER, and federal caution statements about habit-forming potential and transfer restrictions. Storage instructions and other manufacturing details are also present.*
FDA Label Image

Acetaminophen Structure (C87671eb 3ec7 4930 Be25 5686a75679de 01)

Acetaminophen Structure (C87671eb 3ec7 4930 Be25 5686a75679de 01)
Chemical structure of Acetaminophen and Codeine Phosphate, showing a benzene ring with hydroxyl and amide functional groups attached.*
FDA Label Image

Codeine Phosphate Structure (C87671eb 3ec7 4930 Be25 5686a75679de 02)

Codeine Phosphate Structure (C87671eb 3ec7 4930 Be25 5686a75679de 02)
Chemical structure of Acetaminophen and Codeine Phosphate, showing molecular bonds and annotations including H3PO4ยท1/2H2O indicating the presence of phosphoric acid and water of hydration.*

* 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.