Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 202211

OXYTROL FOR WOMEN (OXYBUTYNIN)
3.9MG/24HR Marketing Status: Over-the-counter

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: ALLERGAN SALES LLC
Marketing Status:  Over-the-counter
Patent and Exclusivity Information

Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English