Package 0024-1171-90

Brand: plavix

Generic: clopidogrel
NDC Package

Package Facts

Identity

Package NDC 0024-1171-90
Digits Only 0024117190
Product NDC 0024-1171
Description

90 TABLET, FILM COATED in 1 BOTTLE (0024-1171-90)

Marketing

Marketing Status
Marketed Since 2020-07-13
Brand plavix
Generic clopidogrel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ed60a9e7-49f4-469c-bb7a-08e1bb6057e2", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["213169", "309362", "749196", "749198"], "spl_set_id": ["de8b0b67-eb25-4684-83b5-7ad785314227"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0024-1171-90)", "package_ndc": "0024-1171-90", "marketing_start_date": "20200713"}], "brand_name": "Plavix", "product_id": "0024-1171_ed60a9e7-49f4-469c-bb7a-08e1bb6057e2", "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": "0024-1171", "generic_name": "clopidogrel", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Plavix", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "NDA020839", "marketing_category": "NDA", "marketing_start_date": "19971117", "listing_expiration_date": "20261231"}