Active Ingredient: ISOPROTERENOL HYDROCHLORIDE
Proprietary Name: ISUPREL
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006327
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information