# Chlorpromazine Hydrochloride

NDC: 0527-2965
Generic name: Chlorpromazine Hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20210122

FDA application: ANDA212996

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-2965"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-2965
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1049538a-c012-41bf-932e-3c85f57f9577