# Fluoxetine

NDC: 68001-670
Generic name: Fluoxetine
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20251205

FDA application: ANDA078619

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-670"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-670
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=daf33244-1348-4c34-b44c-9e35d5c48a3e