Package 68071-4138-3
Brand: clopidogrel
Generic: clopidogrelPackage Facts
Identity
Package NDC
68071-4138-3
Digits Only
6807141383
Product NDC
68071-4138
Description
30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)
Marketing
Marketing Status
Brand
clopidogrel
Generic
clopidogrel
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["5cdca9bd-7042-142a-e053-2991aa0a9ca6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)", "package_ndc": "68071-4138-3", "marketing_start_date": "20171031"}], "brand_name": "Clopidogrel", "product_id": "68071-4138_2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5", "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": "68071-4138", "generic_name": "Clopidogrel", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA076999", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}