# Eltrombopag Olamine

NDC: 60219-1415
Generic name: Eltrombopag
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260115

FDA application: ANDA212884

## Active ingredients

- ELTROMBOPAG OLAMINE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60219-1415"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60219-1415
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=05acf38e-7870-4809-a045-fc38e66b1110