NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1927Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1927Add 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
70771-1927-37077119270330 TABLET in 1 BOTTLE (70771-1927-3)Marketed from Jan 14, 2026
70771-1927-77077119270714 TABLET in 1 BOTTLE (70771-1927-7)Marketed from Jan 14, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Active ingredients
Eltrombopag olamine50 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216281
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 70771-1927_5273da92-fa13-4b26-b32f-63955b1983c3SPL ID 5273da92-fa13-4b26-b32f-63955b1983c3SPL set ID ae9a7725-64f8-406d-88e7-e6e01136deaeRxCUI 825421, 825427, 884617, 1245001UNII 4U07F515LG
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

N470771192703 followed by a unit qualifier and the quantity

Package 70771-1927-03. 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 .

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 216281

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

FDA NDC Directory listings under ANDA 216281
ProductStrengthForm · routeLabelerProduct NDC
EltrombopagEltrombopag olamine 75 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1398
EltrombopagEltrombopag olamine 12.5 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1395
EltrombopagEltrombopag olamine 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1396
EltrombopagEltrombopag olamine 50 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1397
EltrombopagEltrombopag olamine 12.5 mg/1TabletOralZydus Lifesciences Limited70771-1925
EltrombopagEltrombopag olamine 25 mg/1TabletOralZydus Lifesciences Limited70771-1926
EltrombopagEltrombopag olamine 75 mg/1TabletOralZydus Lifesciences Limited70771-1928

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