Active Ingredient: PAROXETINE HYDROCHLORIDE
Proprietary Name: PAROXETINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 12.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209748
Product Number: 001
Approval Date: Jan 4, 2024
Applicant Holder Full Name: PRINSTON PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information