Active Ingredient: IVABRADINE HYDROCHLORIDE
Proprietary Name: IVABRADINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 7.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214051
Product Number: 002
Approval Date: Dec 30, 2021
Applicant Holder Full Name: INGENUS PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
