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. Forty 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 |
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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