Details for New Drug Application (NDA): 207329
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The generic ingredient in OXYBUTYNIN CHLORIDE is oxybutynin chloride. There are sixteen drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the oxybutynin chloride profile page.
Summary for 207329
Tradename: | OXYBUTYNIN CHLORIDE |
Applicant: | Chartwell Rx |
Ingredient: | oxybutynin chloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | GEL;TRANSDERMAL | Strength | 10% (100MG/PACKET) | ||||
Approval Date: | May 31, 2018 | TE: | RLD: | No |
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