Oxybutynin Chloride Tablet
Product Images NDC 72789-417

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 72789-417). 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

72789417 Label (72789417)

This medication may cause drowsiness so it is advised not to consume alcohol while taking it. It contains oxybutynin chloride USP, 5mg per tablet. The NDC for this medication is 72789-417-90. The medication comes in white color with a lot number F24D59. The packaging includes 50 tablets per bottle. The recommended dosage and storage instructions can be found in the package insert. Remember to keep this medication out of the reach of children. If you experience any side effects, contact your doctor or report them to the FDA at 1-800-FDA-1088. Each tablet should be taken a certain number of times per day.*

FDA Label Image

Figure 1 (Oxybutynin Figure1)

FDA Label Image

Figure 2 (Oxybutynin Figure2)

FDA Label Image

Structure (Oxybutynin Structure)

Not available.*

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