# Fluoxetine

NDC: 0121-4721
Generic name: FLUOXETINE HYDROCHLORIDE
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20020201

FDA application: ANDA076015

## 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:"0121-4721"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-4721
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=180a07fd-1f6a-4617-b8e0-f938c65ba273