Package 59630-551-07

Brand: mulpleta

Generic: lusutrombopag
NDC Package

Package Facts

Identity

Package NDC 59630-551-07
Digits Only 5963055107
Product NDC 59630-551
Description

1 DOSE PACK in 1 CARTON (59630-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2018-08-27
Brand mulpleta
Generic lusutrombopag
Sample Package No

Linked Drug Pages (1)

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"}