# Thioridazine Hydrochloride

NDC: 53489-148
Generic name: Thioridazine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19881007

FDA application: ANDA089953

## Active ingredients

- THIORIDAZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c4bedb4-2d59-4fcd-aad7-fce988cd96d8