Active Ingredient: AMIODARONE HYDROCHLORIDE
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076362
Product Number: 001
Approval Date: Nov 29, 2002
Applicant Holder Full Name: TARO PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information