Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: FLUOXETINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 60MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211282
Product Number: 001
Approval Date: Jan 10, 2019
Applicant Holder Full Name: SCIEGEN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information