# Fluphenazine Hydrochloride

NDC: 43598-034
Generic name: Fluphenazine Hydrochloride
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210215

FDA application: ANDA214534

## 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:"43598-034"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-034
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98aeddfd-4f24-4d1a-820d-d0abc1733794