# PROMACTA

NDC: 0078-0685
Generic name: eltrombopag olamine
Labeler / Manufacturer: Novartis Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160524

FDA application: NDA022291

## Active ingredients

- ELTROMBOPAG OLAMINE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0078-0685"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0078-0685
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7714a0ed-34bb-46e6-a0a5-b363908b22c2