# PROCHLORPERAZINE MALEATE

NDC: 51655-096
Generic name: Prochlorperazine Maleate
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140428

FDA application: ANDA040268

## Active ingredients

- PROCHLORPERAZINE MALEATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-096"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-096
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c524a28e-1e08-4aa6-a9f0-0a3280a3c213