# Fluphenazine hydrochloride

NDC: 27241-255
Generic name: Fluphenazine hydrochloride
Labeler / Manufacturer: Ajanta Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230105

FDA application: ANDA217410

## Active ingredients

- FLUPHENAZINE HYDROCHLORIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27241-255"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27241-255
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47695e20-9c0b-4a6b-ab1a-1dfaa75e96d8