Package 82009-182-05

Brand: clopidogrel bisulfate

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 82009-182-05
Digits Only 8200918205
Product NDC 82009-182
Description

500 TABLET, FILM COATED in 1 BOTTLE (82009-182-05)

Marketing

Marketing Status
Marketed Since 2025-09-05
Brand clopidogrel bisulfate
Generic clopidogrel bisulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b225308c-50b5-6c91-fc03-1506c1b2dedc", "openfda": {"upc": ["0382009182056"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["d072b6ea-2bb4-8965-918e-23f9080efcb0"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (82009-182-05)", "package_ndc": "82009-182-05", "marketing_start_date": "20250905"}], "brand_name": "Clopidogrel bisulfate", "product_id": "82009-182_b225308c-50b5-6c91-fc03-1506c1b2dedc", "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": "82009-182", "generic_name": "Clopidogrel bisulfate", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel bisulfate", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA091023", "marketing_category": "ANDA", "marketing_start_date": "20250905", "listing_expiration_date": "20261231"}