Package 68645-590-90

Brand: clopidogrel

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 68645-590-90
Digits Only 6864559090
Product NDC 68645-590
Description

90 TABLET, FILM COATED in 1 BOTTLE (68645-590-90)

Marketing

Marketing Status
Marketed Since 2012-05-17
Brand clopidogrel
Generic clopidogrel bisulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c21fe89-421c-249a-e063-6294a90aad2c", "openfda": {"upc": ["0368645590905"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["53de10a5-dbd0-413d-90e5-00a1920ec391"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68645-590-90)", "package_ndc": "68645-590-90", "marketing_start_date": "20120517"}], "brand_name": "Clopidogrel", "product_id": "68645-590_4c21fe89-421c-249a-e063-6294a90aad2c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "68645-590", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA090540", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20271231"}