# Fluoxetine

NDC: 0615-8183
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20080131
Marketing ended: 20261031
FDA application: ANDA078619

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8183"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8183
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f069b9b-16e4-4f0e-b420-4aa02ffbb632