# Tizanidine

NDC: 57664-503
Generic name: Tizanidine
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20031211

FDA application: ANDA076416

## Active ingredients

- TIZANIDINE HYDROCHLORIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-503"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-503
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4659df31-8b89-4eff-9d86-7b7e38de416b