Package 50090-7467-0

Brand: clopidogrel

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 50090-7467-0
Digits Only 5009074670
Product NDC 50090-7467
Product ID 50090-7467_8aa46e42-a9f3-4913-bf64-4226103b6e1b
Description

90 TABLET in 1 BOTTLE (50090-7467-0)

Marketing

Marketing Status
Marketed Since 2024-12-02
Brand clopidogrel
Generic clopidogrel bisulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8aa46e42-a9f3-4913-bf64-4226103b6e1b", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["ffeb2fca-d475-4d93-913d-0048ff9fcee9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7467-0)", "package_ndc": "50090-7467-0", "marketing_start_date": "20241202"}], "brand_name": "CLOPIDOGREL", "product_id": "50090-7467_8aa46e42-a9f3-4913-bf64-4226103b6e1b", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "50090-7467", "generic_name": "CLOPIDOGREL BISULFATE", "labeler_name": "A-S Medication Solutions", "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": "20240516", "listing_expiration_date": "20261231"}