Package 65162-002-03
Brand: prasugrel
Generic: prasugrelPackage Facts
Identity
Package NDC
65162-002-03
Digits Only
6516200203
Product NDC
65162-002
Description
30 TABLET, FILM COATED in 1 BOTTLE (65162-002-03)
Marketing
Marketing Status
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": "ae5f7419-c5fe-4462-8f0e-ffc08e891cd0", "openfda": {"upc": ["0365162002034", "0365162001037"], "unii": ["G89JQ59I13"], "rxcui": ["855812", "855818"], "spl_set_id": ["406cc201-89b6-43cc-9e14-a59327a5b4d8"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65162-002-03)", "package_ndc": "65162-002-03", "marketing_start_date": "20180622"}], "brand_name": "Prasugrel", "product_id": "65162-002_ae5f7419-c5fe-4462-8f0e-ffc08e891cd0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "65162-002", "generic_name": "Prasugrel", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prasugrel", "active_ingredients": [{"name": "PRASUGREL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205913", "marketing_category": "ANDA", "marketing_start_date": "20180622", "listing_expiration_date": "20261231"}