Active Ingredient: ISOPROTERENOL HYDROCHLORIDE
Proprietary Name: ISUPREL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.2MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N010515
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information