# PROZAC WEEKLY
> **NDA021235** · New Drug Application · Sponsor: LILLY · Approved 2001-02-26
## Drug
- **FDA Application Number:** NDA021235
- **Application type:** New Drug Application
- **Brand name:** PROZAC WEEKLY
- **Generic name:** Fluoxetine Hydrochloride
- **Active ingredients:** FLUOXETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE, DELAYED REL PELLETS
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** LILLY
- **First approval:** 2001-02-26
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=021235)
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