Active Ingredient: TOLAZOLINE HYDROCHLORIDE
Proprietary Name: PRISCOLINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006403
Product Number: 005
Approval Date: Feb 22, 1985
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information