Oxybutynin Chloride Tablet, Extended Release
Product Images NDC 71205-667

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 71205-667). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Figure 1 (Oxybutynin Fig 1)

Figure 1 (Oxybutynin Fig 1)
FDA Label Image

Figure 2 (Oxybutynin Fig 2)

Figure 2 (Oxybutynin Fig 2)
FDA Label Image

Figure 3 (Oxybutynin Fig Study 1)

Figure 3 (Oxybutynin Fig Study 1)
FDA Label Image

Figure 4 (Oxybutynin Fig Study 2)

Figure 4 (Oxybutynin Fig Study 2)
FDA Label Image

Figure 5 (Oxybutynin Fig Study 3)

Figure 5 (Oxybutynin Fig Study 3)
FDA Label Image

71205-667-30 (Oxybutynin Lab 10mg)

71205-667-30 (Oxybutynin Lab 10mg)
This is a label of a medication bottle containing 30 extended-release tablets of Oxybutynin Chloride 10mg, manufactured by Proficient Rx LP, Thousand Oaks, CA 91320. The tablets are pink with "EM2" imprinted on one side with black ink. The medication should be stored at 25°C (77°F) and kept away from children. The lot number is 00000, and the expiration date is 00/00/00. The NDC number is 71205-667-30. It is a prescription drug.*
FDA Label Image

Chemical Structure (Oxybutynin Struc)

Chemical Structure (Oxybutynin Struc)

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