Prescription drug · NDA
Mulpleta (Lusutrombopag) NDC 84230-551
Lusutrombopag 3 mg/1 · Tablet, Film coated · Oral · VANCOCIN ITALIA SRL
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 84230-551-07 | 84230055107 | 1 DOSE PACK in 1 CARTON (84230-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACKMarketed from Dec 9, 2025 |
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)
- Mulpleta
- Generic name (nonproprietary)
- lusutrombopag
- Active ingredients
- Lusutrombopag — 3 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- VANCOCIN ITALIA SRLNDC labeler code 84230
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 210923
- Marketing start
- Listing expires
- Identifiers
- Product ID 84230-551_2a019a0b-29c4-d5ef-e063-6394a90ad52fSPL ID 2a019a0b-29c4-d5ef-e063-6394a90ad52fSPL set ID a390aec3-6e77-45f8-95d3-d4b8c2eeee40RxCUI 2054989, 2054995UNII 6LL5JFU42F
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
N484230055107followed by a unit qualifier and the quantityPackage 84230-0551-07. 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 .
Indications (excerpt from the label)
MULPLETA is indicated for the treatment of thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure. MULPLETA is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 84230-551
- What is NDC 84230-551?
- 84230-551 is the product NDC for Mulpleta (lusutrombopag), Lusutrombopag 3 mg/1 tablet, film coated, listed with the FDA by VANCOCIN ITALIA SRL. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Mulpleta (Lusutrombopag).
- What is the active ingredient?
- Lusutrombopag.
- Who is the labeler?
- VANCOCIN ITALIA SRL, NDC labeler code 84230. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Mulpleta?
- 2 other product NDCs are listed under this name. See all Mulpleta NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Mulpleta products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Mulpletalusutrombopag | Lusutrombopag 3 mg/1 | Tablet, Film coatedOral | Eddingpharm (U. S. ) Inc. | 85320-551 | 85320-0551-07 |
| Mulpletalusutrombopag | Lusutrombopag 3 mg/1 | Tablet, Film coatedOral | SHIONOGI INC. | 59630-551 | 59630-0551-0759630-0551-77 |
Other NDCs under NDA 210923
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Mulpletalusutrombopag | Lusutrombopag 3 mg/1 | Tablet, Film coatedOral | Eddingpharm (U. S. ) Inc. | 85320-551 |
| Mulpletalusutrombopag | Lusutrombopag 3 mg/1 | Tablet, Film coatedOral | SHIONOGI INC. | 59630-551 |