Active Ingredient: DRONEDARONE HYDROCHLORIDE
Proprietary Name: DRONEDARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 400MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A205904
Product Number: 001
Approval Date: Jan 31, 2024
Applicant Holder Full Name: LUPIN INC
Marketing Status:
Prescription
Patent and Exclusivity Information