Active Ingredient: OXYBUTYNIN
Proprietary Name: OXYTROL FOR WOMEN
Dosage Form; Route of Administration: FILM, EXTENDED RELEASE; TRANSDERMAL
Strength: 3.9MG/24HR
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N202211
Product Number: 001
Approval Date: Jan 25, 2013
Applicant Holder Full Name: ABBVIE
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
