# Prochlorperazine Maleate

NDC: 70710-1667
Generic name: Prochlorperazine Maleate
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220810

FDA application: ANDA216495

## 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:"70710-1667"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1667
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4a34138-a01b-418f-8e0f-e81f6e1cfd89