Oxybutynin Chloride Tablet
Product Images NDC 72789-490

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 72789-490). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789490 Label (72789490)

Each tablet of this medication contains D Oxybutynin Chloride, USP 5 mg. The recommended dosage and administration instructions are to take one tablet two to three times a day. The medication should be dispensed in a tightly sealed, light-resistant container and stored at 20°C to 25°C. Additional prescribing information can be found in the package insert. This medication is manufactured by Appco Pharma LLC and marketed by PD-Rx Pharmaceuticals, Inc. It is important to keep this medication out of the reach of children. For inquiries, contact PD-Rx Pharmaceuticals, Inc.*

FDA Label Image

Figure 1 (Oxybutynin Figure1)

FDA Label Image

Figure 2 (Oxybutynin Figure2)

FDA Label Image

Structure (Oxybutynin Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.