# Fluoxetine

NDC: 43063-839
Generic name: Fluoxetine
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160129

FDA application: ANDA090223

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-839"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-839
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=620ecf00-5473-4420-afd1-94b5b38e7301