Active Ingredient: OXYBUTYNIN
Proprietary Name: OXYTROL
Dosage Form; Route of Administration: FILM, EXTENDED RELEASE; TRANSDERMAL
Strength: 3.9MG/24HR
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N021351
Product Number: 002
Approval Date: Feb 26, 2003
Applicant Holder Full Name: ALLERGAN SALES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
