# Chlorpromazine Hydrochloride

NDC: 70518-3549
Generic name: Chlorpromazine Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, SUGAR COATED
Routes: ORAL
Marketing started: 20221003

FDA application: ANDA214827

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3549"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3549
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2a38be8-43e6-4a56-9556-fe3dad412b82