Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: FLUOXETINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A076006
Product Number: 002
Approval Date: Apr 23, 2018
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information