# FLUOXETINE

NDC: 64380-902
Generic name: fluoxetine
Labeler / Manufacturer: Strides Pharma Science Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240812

FDA application: ANDA212684

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64380-902"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64380-902
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca749349-d0e1-4b7c-b4c0-e392e72cf0f6