# Fluoxetine

NDC: 16714-722
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: NorthStar Rx LLC
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: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-722"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-722
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97960730-432e-4e94-bb4e-62a3157270a8