# PROCHLORPERAZINE MALEATE

NDC: 69315-266
Generic name: PROCHLORPERAZINE MALEATE
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250625

FDA application: ANDA218912

## Active ingredients

- PROCHLORPERAZINE MALEATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-266"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-266
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c93494ef-c510-4e46-a1b1-362624200223