Active Ingredient: FOSAMPRENAVIR CALCIUM
Proprietary Name: FOSAMPRENAVIR CALCIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 700MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204024
Product Number: 001
Approval Date: Nov 20, 2019
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information