# Fluoxetine

NDC: 54838-523
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: ORAL
Marketing started: 20090827

FDA application: ANDA077849

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 20 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54838-523"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54838-523
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c856d72f-4a1a-4f75-ae54-c4ac83ddcfa1