Active Ingredient: IPTACOPAN HYDROCHLORIDE
Proprietary Name: FABHALTA
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 200MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N218276
Product Number: 001
Approval Date: Dec 5, 2023
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Prescription
Patent and Exclusivity Information