Oxybutynin Chloride Tablet, Extended Release
Product Images NDC 62175-271
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Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 62175-271). 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.
Product Images & Figures Index
Oxybutynin Chloride Extended Release 2
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Oxybutynin Chloride Extended Release 7
This appears to be a medication label, indicating details about a drug called Oxybutynin Chloride. The dosage level is stated as "Extended-Release" and the form of the medication is tablets. It should be stored at a temperature between 15°C and 30°C and protected from moisture and humidity. The medication is manufactured by a company with the code "62175-270-37".*
Oxybutynin Chloride Extended Release 8
Oxybutynin Chloride Extended Release 9
Each tablet of Oxybutynin Chloride Extended-Release USP formulation contains 15 mg oxybutynin chloride. The recommended dose is one tablet per day. For more information about dosing, please refer to the package insert. It is advised to store the tablet at a temperature not exceeding 25°C (77°F) with excursions permitted to 15%-30°C (59°-86°F) as per USP Controlled Room Temperatures. Protect the tablet from moisture and humidity. The product is marked with the number NOC 6217527237 and the revision date is CATZ807F Rev. 10/19.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.