# Fluoxetine

NDC: 60687-845
Generic name: Fluoxetine
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20241204

FDA application: ANDA079209

## 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:"60687-845"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-845
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3276a2a4-61c7-4de6-b519-3aa8b62da88f