# PROCHLORPERAZINE MALEATE

NDC: 68462-947
Generic name: PROCHLORPERAZINE MALEATE
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250528

FDA application: ANDA216595

## 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:"68462-947"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-947
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c806152-70d0-43eb-b183-b51b12b82b31