# Fluoxetine

NDC: 68999-730
Generic name: Fluoxetine
Labeler / Manufacturer: Chartwell Governmental & Specialty RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: ORAL
Marketing started: 20040514

FDA application: ANDA076458

## 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:"68999-730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-730
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d34362ed-e821-4c55-9f8c-3dfb772b1b2a