Package 0378-5186-93

Brand: prasugrel

Generic: prasugrel
NDC Package

Package Facts

Identity

Package NDC 0378-5186-93
Digits Only 0378518693
Product NDC 0378-5186
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5186-93)

Marketing

Marketing Status
Marketed Since 2017-08-15
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": "9e234352-49b7-46e3-bc59-acf63e0a7a14", "openfda": {"upc": ["0303785185932"], "unii": ["G89JQ59I13"], "rxcui": ["855812", "855818"], "spl_set_id": ["41a4e332-6725-4cb7-940a-8291cf56cfe4"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5186-93)", "package_ndc": "0378-5186-93", "marketing_start_date": "20170815"}], "brand_name": "Prasugrel", "product_id": "0378-5186_9e234352-49b7-46e3-bc59-acf63e0a7a14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "0378-5186", "generic_name": "Prasugrel", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prasugrel", "active_ingredients": [{"name": "PRASUGREL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205927", "marketing_category": "ANDA", "marketing_start_date": "20170815", "listing_expiration_date": "20261231"}