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  5. NDC Package Code: 85320-551-07 Mulpleta

NDC Package 85320-551-07 Mulpleta

Lusutrombopag Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
85320-551-07
Package Description:
1 DOSE PACK in 1 CARTON / 7 TABLET, FILM COATED in 1 DOSE PACK
Product Code:
85320-551
Proprietary Name:
Mulpleta
Non-Proprietary Name:
Lusutrombopag
Substance Name:
Lusutrombopag
Usage Information:
This medication is used by people with chronic liver disease and a certain blood disorder (low platelet count) who are scheduled to have a medical or dental procedure. Having a low platelet count increases the risk of too much bleeding during certain procedures. This medication increases the production of platelets by your body to help prevent too much bleeding from the procedure.
11-Digit NDC Billing Format:
85320055107
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Eddingpharm (u. S. ) Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
LUSUTROMBOPAG 3 mg/1
Sample Package:
No
FDA Application Number:
NDA210923
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
11-24-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 85320-551-07?

The NDC Packaged Code 85320-551-07 is assigned to a package of 1 dose pack in 1 carton / 7 tablet, film coated in 1 dose pack of Mulpleta, a human prescription drug labeled by Eddingpharm (u. S. ) Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 85320-551 included in the NDC Directory?

Yes, Mulpleta with product code 85320-551 is active and included in the NDC Directory. The product was first marketed by Eddingpharm (u. S. ) Inc. on November 24, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 85320-551-07?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 85320-551-07?

The 11-digit format is 85320055107. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-285320-551-075-4-285320-0551-07