Oxybutynin Chloride Syrup
Product Images NDC 54838-510

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 Oxybutynin Chloride (NDC 54838-510). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structure Of Oxybutynin (Oxybutynin Chloride 1)

FDA Label Image

Figure 1 (Oxybutynin Chloride 2)

Figure 1 (Oxybutynin Chloride 2)
This appears to be a medication prescription for Oxybutynin at a dose of 5 mg to be taken three times a day. The rest of the text is not readable and cannot be used to generate a useful description.*
FDA Label Image

Figure 1 (Oxybutynin Chloride 3)

Figure 1 (Oxybutynin Chloride 3)
This text presents a comparison of the mean plasma concentration of R-Oxybutynin in patients taking Oxybutynin Chloride Syrup 5mg and Oxybutynin Chloride IR Tablet 5mg over time.*
FDA Label Image

5 mg Per 5 mL (Oxybutynin Chloride 4)

5 mg Per 5 mL (Oxybutynin Chloride 4)
NDC 54636-510:80 is a syrup medication with oxibutynin chloride as the active ingredient, used to treat symptoms of an overactive bladder such as frequent urination, urgent need to urinate or incontinence. It contains 5 mg of oxybutynin chloride in each teaspoonful. The usual dosage and safety information is provided in the text. This medication comes in a 1 pint (473 mL) bottle only available with a prescription.*

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