Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: FLUOXETINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 20MG BASE/5ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AA
Application Number: A076015
Product Number: 001
Approval Date: Jan 30, 2002
Applicant Holder Full Name: PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Prescription
Patent and Exclusivity Information