# CHLORPROMAZINE HYDROCHLORIDE

NDC: 60687-452
Generic name: CHLORPROMAZINE HYDROCHLORIDE
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190516

FDA application: ANDA209755

## Active ingredients

- CHLORPROMAZINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-452"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-452
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d43718e5-66d7-44f9-9fc8-80d38d3e41ce