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Active Ingredient: PRASUGREL HYDROCHLORIDE
Proprietary Name: PRASUGREL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206021
Product Number: 001
Approval Date: Jan 16, 2019
Applicant Holder Full Name: HEC PHARM USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
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: A206021
Product Number: 002
Approval Date: Jan 16, 2019
Applicant Holder Full Name: HEC PHARM USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
