Hydrocodone Polistirex And Chlorpheniramine Polistirex Suspension, Extended Release
Product Images NDC 63629-2303

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Polistirex And Chlorpheniramine Polistirex (NDC 63629-2303). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure 1 (Hydrocodone Polistirex And Chlorpheniramine Polist 1)

FDA Label Image

Structure 2 (Hydrocodone Polistirex And Chlorpheniramine Polist 2)

FDA Label Image

Cup (Hydrocodone Polistirex And Chlorpheniramine Polist 3)

Cup (Hydrocodone Polistirex And Chlorpheniramine Polist 3)
This text provides a conversion chart for teaspoons and milliliters. 1 teaspoon is equivalent to 5 milliliters and 0.5 teaspoon is equivalent to 2.5 milliliters.*
FDA Label Image

Label (Lbl636292303)

Label (Lbl636292303)
Hydrocodone Polistirex and Chlorpheniramine Polistirex ER Suspension is a prescription-only medication containing 10 mg/5ml of Hydrocodone Bitartrate, USP, and 8 mg/5ml of Chlorpheniramine Maleate, USP in a 115 mL bottle. It is essential to keep this medication out of reach of children and store it at a controlled room temperature of 20° to 25°C (68° to 77°F) in a tightly closed light-resistant container. This medication may cause drowsiness. NILD is an unidentified entity, and Aq pajaqeley and Aq painjoejnuey are not understandable.*

* 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.