# Thioridazine Hydrochloride

NDC: 0378-0618
Generic name: thioridazine hydrochloride
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19831118

FDA application: ANDA088004

## Active ingredients

- THIORIDAZINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-0618"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-0618
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56b3f4c2-52af-4947-b225-6808ae9f26f5