# Fluoxetine

NDC: 42708-025
Generic name: Fluoxetine
Labeler / Manufacturer: QPharma Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20020129

FDA application: ANDA076001

## 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:"42708-025"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-025
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4831735-6731-473a-b4f0-1f4a67aa7120