# Fluoxetine

NDC: 68645-130
Generic name: Fluoxetine
Labeler / Manufacturer: Legacy Pharmaceutical Packaging, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20110125

FDA application: ANDA076001

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68645-130"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68645-130
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b07f9eab-44ac-4667-bd46-52d736daa5d6