Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021235

PROZAC WEEKLY (FLUOXETINE HYDROCHLORIDE)
EQ 90MG BASE
Marketing Status: Discontinued
Active Ingredient: FLUOXETINE HYDROCHLORIDE
Proprietary Name: PROZAC WEEKLY
Dosage Form; Route of Administration: CAPSULE, DELAYED REL PELLETS; ORAL
Strength: EQ 90MG BASE
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

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