Active Ingredient: PRASUGREL HYDROCHLORIDE
Proprietary Name: PRASUGREL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A205913
Product Number: 002
Approval Date: Jun 19, 2018
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS OF NEW YORK LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
