Package 84230-551-07

Brand: mulpleta

Generic: lusutrombopag
NDC Package

Package Facts

Identity

Package NDC 84230-551-07
Digits Only 8423055107
Product NDC 84230-551
Description

1 DOSE PACK in 1 CARTON (84230-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2025-12-09
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": "2a019a0b-29c4-d5ef-e063-6394a90ad52f", "openfda": {"unii": ["6LL5JFU42F"], "rxcui": ["2054989", "2054995"], "spl_set_id": ["a390aec3-6e77-45f8-95d3-d4b8c2eeee40"], "manufacturer_name": ["VANCOCIN ITALIA SRL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (84230-551-07)  / 7 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "84230-551-07", "marketing_start_date": "20251209"}], "brand_name": "Mulpleta", "product_id": "84230-551_2a019a0b-29c4-d5ef-e063-6394a90ad52f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "84230-551", "generic_name": "Lusutrombopag", "labeler_name": "VANCOCIN ITALIA SRL", "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": "20251209", "listing_expiration_date": "20261231"}