# Fluoxetine

NDC: 50090-6065
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20080131

FDA application: ANDA078619

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6065"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6065
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1226a67f-ec09-42f6-9d1b-9ddd862ea0a0