NDC codes

FDA NDC Directory
Product NDC (as listed)72205-159Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72205-0159Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
72205-159-307220501593030 TABLET, FILM COATED in 1 BOTTLE (72205-159-30)Marketed from Jan 14, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
eltrombopag
Generic name (nonproprietary)
eltrombopag olamine
Active ingredients
Eltrombopag olamine — 75 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220250
Marketing start
Listing expires
Other FDA classes
Breast Cancer Resistance Protein Inhibitors (Mechanism)Increased Megakaryocyte Maturation (Physiologic effect)Increased Platelet Production (Physiologic effect)Organic Anion Transporting Polypeptide 1B1 Inhibitors (Mechanism)Thrombopoietin Receptor Agonists (Mechanism)UGT1A1 Inhibitors (Mechanism)UGT1A3 Inhibitors (Mechanism)UGT1A4 Inhibitors (Mechanism)UGT1A6 Inhibitors (Mechanism)UGT1A9 Inhibitors (Mechanism)UGT2B15 Inhibitors (Mechanism)UGT2B7 Inhibitors (Mechanism)
Identifiers
Product ID 72205-159_5a9ec8c8-3c0b-4f11-848c-c04ccee0d44fSPL ID 5a9ec8c8-3c0b-4f11-848c-c04ccee0d44fSPL set ID 5a9ec8c8-3c0b-4f11-848c-c04ccee0d44fRxCUI 825421, 825427, 884617, 1245001UNII 4U07F515LGUPC 0372205159303, 0372205158191, 0372205157309, 0372205158306
Pharmacologic class
Thrombopoietin Receptor Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472205015930 followed by a unit qualifier and the quantity

Package 72205-0159-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Eltrombopag tablets are a thrombopoietin receptor agonist indicated: for the treatment of thrombocytopenia in adult and pediatric patients 1 year and older with persistent or chronic immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. Eltrombopag tablets should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increase the risk for bleeding. ( 1.1 ) for the treatment of thrombocytopenia in patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy. Eltrombopag tablets should be used only in patients with chronic hepatitis C whose degree of th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 220250

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 220250
ProductStrengthForm · routeLabelerProduct NDC
eltrombopageltrombopag olamineEltrombopag olamine 50 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-158
eltrombopageltrombopag olamineEltrombopag olamine 25 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-157
eltrombopageltrombopag olamineEltrombopag olamine 12.5 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-156

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