# Fluoxetine Hydrochloride

NDC: 70954-600
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20221109

FDA application: ANDA216448

## 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:"70954-600"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-600
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1ffe57c3-6f70-4075-aacb-d87a3990fdea