# Chlorpromazine hydrochloride

NDC: 16714-048
Generic name: Chlorpromazine hydrochloride
Labeler / Manufacturer: Northstar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200511

FDA application: ANDA213368

## 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:"16714-048"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-048
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2bd42d3a-bf89-4d74-a252-9b914106a570