Package 43817-240-01

Brand: prasugrel

Generic: prasugrel
NDC Package

Package Facts

Identity

Package NDC 43817-240-01
Digits Only 4381724001
Product NDC 43817-240
Description

30 TABLET, FILM COATED in 1 BOTTLE (43817-240-01)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand prasugrel
Generic prasugrel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2de10117-c50f-95af-e063-6294a90ab07d", "openfda": {"unii": ["G89JQ59I13"], "rxcui": ["855812", "855818"], "spl_set_id": ["944c195a-de24-a44c-8baa-84b624b5ddcb"], "manufacturer_name": ["Panacea Biotec Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43817-240-01)", "package_ndc": "43817-240-01", "marketing_end_date": "20261031", "marketing_start_date": "20171016"}], "brand_name": "PRASUGREL", "product_id": "43817-240_2de10117-c50f-95af-e063-6294a90ab07d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "43817-240", "generic_name": "PRASUGREL", "labeler_name": "Panacea Biotec Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRASUGREL", "active_ingredients": [{"name": "PRASUGREL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205897", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20171016"}