mulpleta

Generic: lusutrombopag

Labeler: shionogi inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name mulpleta
Generic Name lusutrombopag
Labeler shionogi inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lusutrombopag 3 mg/1

Manufacturer
SHIONOGI INC.

Identifiers & Regulatory

Product NDC 59630-551
Product ID 59630-551_b520c88c-9064-4ffe-b33c-81fdfe795cad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA210923
Listing Expiration 2026-12-31
Marketing Start 2018-08-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59630551
Hyphenated Format 59630-551

Supplemental Identifiers

RxCUI
2054989 2054995
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 (59630-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK
  • 1 DOSE PACK in 1 CARTON (59630-551-77) / 7 TABLET, FILM COATED in 1 DOSE PACK
source: ndc

Packages (2)

59630-551-07 1 DOSE PACK in 1 CARTON (59630-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK 59630-551-77 1 DOSE PACK in 1 CARTON (59630-551-77) / 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": "b520c88c-9064-4ffe-b33c-81fdfe795cad", "openfda": {"unii": ["6LL5JFU42F"], "rxcui": ["2054989", "2054995"], "spl_set_id": ["f9fd0cfd-717d-4a87-99bc-de7b38807e55"], "manufacturer_name": ["SHIONOGI INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (59630-551-07)  / 7 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "59630-551-07", "marketing_start_date": "20180827"}, {"sample": true, "description": "1 DOSE PACK in 1 CARTON (59630-551-77)  / 7 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "59630-551-77", "marketing_start_date": "20180827"}], "brand_name": "Mulpleta", "product_id": "59630-551_b520c88c-9064-4ffe-b33c-81fdfe795cad", "dosage_form": "TABLET, FILM COATED", "product_ndc": "59630-551", "generic_name": "Lusutrombopag", "labeler_name": "SHIONOGI 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": "20180827", "listing_expiration_date": "20261231"}