# Fluoxetine

NDC: 43063-993
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20080131

FDA application: ANDA078619

## 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:"43063-993"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-993
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a5fa64a6-3de3-4e2e-8b92-6d507fb8eee9