Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: FLUOXETINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075755
Product Number: 001
Approval Date: Aug 2, 2001
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:
Discontinued
Patent and Exclusivity Information