Eltrombopag olamine
NDC 70069-837, Eltrombopag olamine, tablet, film coated, from Somerset Therapeutics, LLC.
- Product NDC
- 70069-837
- Status
- Listed
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219638
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70069-837 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ELTROMBOPAG OLAMINE12.5 mg/1
Pharmacologic classes
Breast Cancer Resistance Protein Inhibitors [MoA]; Increased Megakaryocyte Maturation [PE]; Increased Platelet Production [PE]; Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA]; Thrombopoietin Receptor Agonist [EPC]; Thrombopoietin Receptor Agonists [MoA]; UGT1A1 Inhibitors [MoA]; UGT1A3 Inhibitors [MoA]; UGT1A4 Inhibitors [MoA]; UGT1A6 Inhibitors [MoA]; UGT1A9 Inhibitors [MoA]; UGT2B15 Inhibitors [MoA]; UGT2B7 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70069-837-01 | 70069083701 | 30 TABLET, FILM COATED in 1 BOTTLE (70069-837-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/604f663c-4933-402a-8105-5921713cf3c8
Use it
Look up 70069-837 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70069-837 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70069-837. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.