# FLUOXETINE

NDC: 71656-089
Generic name: FLUOXETINE
Labeler / Manufacturer: Saptalis Pharmaceuticals, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250620

FDA application: ANDA075525

## 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:"71656-089"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71656-089
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4527c502-b28c-449f-ad2d-7daf21563cfa