Package 70518-4373-0
Brand: clopidogrel
Generic: clopidogrel bisulfatePackage Facts
Identity
Package NDC
70518-4373-0
Digits Only
7051843730
Product NDC
70518-4373
Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-4373-0)
Marketing
Marketing Status
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": "388cc422-27df-293f-e063-6394a90a2772", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["669f0bc6-f173-484d-8efe-c006683b25d1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4373-0)", "package_ndc": "70518-4373-0", "marketing_start_date": "20250626"}], "brand_name": "CLOPIDOGREL", "product_id": "70518-4373_388cc422-27df-293f-e063-6394a90a2772", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "70518-4373", "generic_name": "CLOPIDOGREL BISULFATE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOPIDOGREL", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA203632", "marketing_category": "ANDA", "marketing_start_date": "20250626", "listing_expiration_date": "20261231"}