# Fluphenazine Hydrochloride

NDC: 68462-337
Generic name: Fluphenazine Hydrochloride
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231106

FDA application: ANDA216350

## Active ingredients

- FLUPHENAZINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c3eea71-a7a1-4eda-9871-034ddeb83ed6