Active Ingredient: OXYBUTYNIN CHLORIDE
Proprietary Name: OXYBUTYNIN CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209025
Product Number: 001
Approval Date: Dec 21, 2017
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:
Prescription
Patent and Exclusivity Information