Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021351

OXYTROL (OXYBUTYNIN)
3.9MG/24HR Marketing Status: Prescription

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: AB
Application Number: N021351
Product Number: 002
Approval Date: Feb 26, 2003
Applicant Holder Full Name: ALLERGAN SALES LLC
Marketing Status:  Prescription
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