# Prochlorperazine

NDC: 54348-989
Generic name: PROCHLORPERAZINE
Labeler / Manufacturer: PharmPak, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190711

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:"54348-989"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54348-989
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=383744db-ba57-478a-8041-2ecc26d3e1ec