Package 85320-551-07

Brand: mulpleta

Generic: lusutrombopag
NDC Package

Package Facts

Identity

Package NDC 85320-551-07
Digits Only 8532055107
Product NDC 85320-551
Product ID 85320-551_450774dd-f9dc-b934-e063-6294a90a9a6e
Description

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

Marketing

Marketing Status
Marketed Since 2025-11-24
Brand mulpleta
Generic lusutrombopag
Sample Package No

Linked Drug Pages (1)

Mulpleta ndc-match (0.95)

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"}