# Fluphenazine Hydrochloride

NDC: 59651-687
Generic name: Fluphenazine Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230818

FDA application: ANDA218055

## Active ingredients

- FLUPHENAZINE HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-687"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-687
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e73764e7-e666-4ad3-a029-04a528dc1c9e