# CHLORPROMAZINE HYDROCHLORIDE

NDC: 55150-319
Generic name: CHLORPROMAZINE HYDROCHLORIDE
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR
Marketing started: 20200707

FDA application: ANDA211816

## 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:"55150-319"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-319
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07e6144a-b460-4887-b8e2-dd371c14a55c