# Xermelo

NDC: 70183-125
Generic name: telotristat ethyl
Labeler / Manufacturer: Lexicon Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170301

FDA application: NDA208794

## Active ingredients

- TELOTRISTAT ETHYL: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70183-125"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70183-125
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f9108ac3-ca6e-4faf-9d04-953abb64d072