mulpleta

Generic: lusutrombopag

Labeler: eddingpharm (u. s. ) inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name mulpleta
Generic Name lusutrombopag
Labeler eddingpharm (u. s. ) inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lusutrombopag 3 mg/1

Manufacturer
Eddingpharm (U. S. ) Inc.

Identifiers & Regulatory

Product NDC 85320-551
Product ID 85320-551_450774dd-f9dc-b934-e063-6294a90a9a6e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA210923
Listing Expiration 2026-12-31
Marketing Start 2025-11-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85320551
Hyphenated Format 85320-551

Supplemental Identifiers

RxCUI
2054989 2054995
UPC
0385320551075
UNII
6LL5JFU42F

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mulpleta (source: ndc)
Generic Name lusutrombopag (source: ndc)
Application Number NDA210923 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 1 DOSE PACK in 1 CARTON (85320-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK
source: ndc

Packages (1)

85320-551-07 1 DOSE PACK in 1 CARTON (85320-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK

Ingredients (1)

lusutrombopag (3 mg/1)

Linked Drug Pages (1)

Mulpleta ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "450774dd-f9dc-b934-e063-6294a90a9a6e", "openfda": {"upc": ["0385320551075"], "unii": ["6LL5JFU42F"], "rxcui": ["2054989", "2054995"], "spl_set_id": ["3f6b72db-3abc-4169-9bee-8dc3078357e6"], "manufacturer_name": ["Eddingpharm (U. S. ) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (85320-551-07)  / 7 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "85320-551-07", "marketing_start_date": "20251124"}], "brand_name": "Mulpleta", "product_id": "85320-551_450774dd-f9dc-b934-e063-6294a90a9a6e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "85320-551", "generic_name": "Lusutrombopag", "labeler_name": "Eddingpharm (U. S. ) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mulpleta", "active_ingredients": [{"name": "LUSUTROMBOPAG", "strength": "3 mg/1"}], "application_number": "NDA210923", "marketing_category": "NDA", "marketing_start_date": "20251124", "listing_expiration_date": "20261231"}