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: A205927
Product Number: 002
Approval Date: Jul 12, 2017
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
