Package 16729-273-10

Brand: prasugrel

Generic: prasugrel
NDC Package

Package Facts

Identity

Package NDC 16729-273-10
Digits Only 1672927310
Product NDC 16729-273
Product ID 16729-273_0e2f030a-d262-a36c-e063-6294a90a40ef
Description

30 TABLET, FILM COATED in 1 BOTTLE (16729-273-10)

Marketing

Marketing Status
Marketed Since 2019-01-16
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": "0e2f030a-d262-a36c-e063-6294a90a40ef", "openfda": {"unii": ["G89JQ59I13"], "rxcui": ["855812", "855818"], "spl_set_id": ["cd6bf899-06b7-4f52-96c5-ffc94a7288ff"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16729-273-10)", "package_ndc": "16729-273-10", "marketing_start_date": "20190116"}], "brand_name": "Prasugrel", "product_id": "16729-273_0e2f030a-d262-a36c-e063-6294a90a40ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "16729-273", "generic_name": "Prasugrel", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prasugrel", "active_ingredients": [{"name": "PRASUGREL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205987", "marketing_category": "ANDA", "marketing_start_date": "20190116", "listing_expiration_date": "20261231"}