Active Ingredient: BUSPIRONE HYDROCHLORIDE
Proprietary Name: BUSPIRONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078302
Product Number: 001
Approval Date: Dec 17, 2007
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information