# Chlorpromazine Hydrochloride

NDC: 0832-6021
Generic name: Chlorpromazine Hydrochloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110803

FDA application: ANDA084115

## 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:"0832-6021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-6021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5ae79c1e-f523-4358-9f8b-7382a03d59bc