Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075203
Product Number: 001
Approval Date: Oct 24, 2000
Applicant Holder Full Name: WATSON LABORATORIES
Marketing Status:
Prescription
Patent and Exclusivity Information
