# TEPMETKO

NDC: 44087-5000
Generic name: Tepotinib Hydrochloride
Labeler / Manufacturer: EMD Serono, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210203

FDA application: NDA214096

## Active ingredients

- TEPOTINIB HYDROCHLORIDE: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"44087-5000"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=44087-5000
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80a0f1b9-071a-47f5-9e67-32d638a669dc