# TUKYSA

NDC: 51144-002
Generic name: tucatinib
Labeler / Manufacturer: SEAGEN INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200417

FDA application: NDA213411

## Active ingredients

- TUCATINIB: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51144-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51144-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f27eb1b9-b7fc-424e-988f-84dd7bb195a3