Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: PROZAC WEEKLY
Dosage Form; Route of Administration: CAPSULE, DELAYED REL PELLETS; ORAL
Strength: EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021235
Product Number: 001
Approval Date: Feb 26, 2001
Applicant Holder Full Name: ELI LILLY AND CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
