# Fluphenazine Hydrochloride

NDC: 0904-7157
Generic name: Fluphenazine Hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19880825

FDA application: ANDA089743

## Active ingredients

- FLUPHENAZINE HYDROCHLORIDE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7157"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7157
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8d4065a-45fc-4adf-9406-2122ca131d99