Prescription drug · NDA
Mulpleta (Lusutrombopag) NDC 85320-551
Lusutrombopag 3 mg/1 · Tablet, Film coated · Oral · Eddingpharm (U. S. ) Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85320-551-07 | 85320055107 | 1 DOSE PACK in 1 CARTON (85320-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACKMarketed from Nov 24, 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
- Eddingpharm (U. S. ) Inc.NDC labeler code 85320
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 210923
- Marketing start
- Listing expires
- Identifiers
- Product ID 85320-551_450774dd-f9dc-b934-e063-6294a90a9a6eSPL ID 450774dd-f9dc-b934-e063-6294a90a9a6eSPL set ID 3f6b72db-3abc-4169-9bee-8dc3078357e6RxCUI 2054989, 2054995UNII 6LL5JFU42FUPC 0385320551075
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
N485320055107followed by a unit qualifier and the quantityPackage 85320-0551-07. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
About NDC 85320-551
- What is NDC 85320-551?
- 85320-551 is the product NDC for Mulpleta (lusutrombopag), Lusutrombopag 3 mg/1 tablet, film coated, listed with the FDA by Eddingpharm (U. S. ) Inc.. 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?
- Eddingpharm (U. S. ) Inc., NDC labeler code 85320. 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 | VANCOCIN ITALIA SRL | 84230-551 | 84230-0551-07 |
| 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 | SHIONOGI INC. | 59630-551 |
| Mulpletalusutrombopag | Lusutrombopag 3 mg/1 | Tablet, Film coatedOral | VANCOCIN ITALIA SRL | 84230-551 |