# Chlorpromazine Hydrochloride

NDC: 71656-101
Generic name: Chlorpromazine Hydrochloride
Labeler / Manufacturer: Saptalis Pharmaceuticals, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CONCENTRATE
Routes: ORAL
Marketing started: 20260304

FDA application: ANDA080983

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71656-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71656-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd8f9e23-d08a-4d96-8fe9-35ab2bc861c8