# PROCHLORPERAZINE MALEATE

NDC: 69452-472
Generic name: Prochlorperazine Maleate
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250131

FDA application: ANDA217478

## Active ingredients

- PROCHLORPERAZINE MALEATE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-472"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-472
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2cf363d6-b9e4-2c22-e063-6394a90a7649