# Fluoxetine

NDC: 72241-009
Generic name: Fluoxetine
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210908

FDA application: ANDA206993

## 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:"72241-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=05b0781b-50e2-4311-bde0-430b96e2ef8e