Package 0024-1171-90
Brand: plavix
Generic: clopidogrelPackage 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
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"}