Active Ingredient: OXYBUTYNIN CHLORIDE
Proprietary Name: OXYBUTYNIN CHLORIDE
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: 5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075137
Product Number: 001
Approval Date: Dec 18, 1998
Applicant Holder Full Name: PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information