# ChlorproMAZINE Hydrochloride

NDC: 63304-143
Generic name: ChlorproMAZINE
Labeler / Manufacturer: Sun Pharmaceutical Industries Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, SUGAR COATED
Routes: ORAL
Marketing started: 20201118

FDA application: ANDA214256

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-143"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-143
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=432cd4ca-c728-48ff-beec-2485f5e02512