Package 29300-301-13

Brand: prasugrel

Generic: prasugrel
NDC Package

Package Facts

Identity

Package NDC 29300-301-13
Digits Only 2930030113
Product NDC 29300-301
Product ID 29300-301_b60d626b-a3ab-45a0-9abc-cce73f2039da
Description

30 TABLET, FILM COATED in 1 BOTTLE (29300-301-13)

Marketing

Marketing Status
Marketed Since 2023-10-16
Brand prasugrel
Generic prasugrel
Sample Package No

Linked Drug Pages (1)

Prasugrel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b60d626b-a3ab-45a0-9abc-cce73f2039da", "openfda": {"unii": ["G89JQ59I13"], "rxcui": ["855812", "855818"], "spl_set_id": ["5edc1ab3-5c7a-47d6-8aaa-00523c9b4c8f"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (29300-301-13)", "package_ndc": "29300-301-13", "marketing_start_date": "20231016"}], "brand_name": "Prasugrel", "product_id": "29300-301_b60d626b-a3ab-45a0-9abc-cce73f2039da", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "29300-301", "generic_name": "Prasugrel", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prasugrel", "active_ingredients": [{"name": "PRASUGREL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213315", "marketing_category": "ANDA", "marketing_start_date": "20231016", "listing_expiration_date": "20261231"}