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Active Ingredient: PAZOPANIB HYDROCHLORIDE
Proprietary Name: PAZOPANIB HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 200MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A217517
Product Number: 001
Approval Date: Oct 19, 2023
Applicant Holder Full Name: TEVA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
