# CHLORPROMAZINE HYDROCHLORIDE

NDC: 31722-366
Generic name: chlorpromazine hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR
Marketing started: 20241118

FDA application: ANDA218272

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-366"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-366
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6564346c-661c-41cf-9cef-db6aa15710cd