# Chlorpromazine Hydrochloride

NDC: 70710-1850
Generic name: Chlorpromazine Hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR
Marketing started: 20240329

FDA application: ANDA217275

## 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:"70710-1850"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1850
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7cd6dc0d-e98d-40ae-80d4-c15f63056abf