# Fluoxetine

NDC: 17224-174
Generic name: FLUOXETINE HYDROCHLORIDE
Labeler / Manufacturer: Calvin Scott & Co., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20150316

FDA application: ANDA204597

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17224-174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17224-174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4915e22f-cecb-4261-8389-9bb417a20e82