Package 72789-469-90

Brand: clopidogrel

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 72789-469-90
Digits Only 7278946990
Product NDC 72789-469
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-469-90)

Marketing

Marketing Status
Marketed Since 2025-01-02
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": "2abaa65e-cc80-156c-e063-6294a90a44be", "openfda": {"upc": ["0372789469904"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["20247bf8-30ec-4807-95c1-8ec7587368ae"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-469-90)", "package_ndc": "72789-469-90", "marketing_start_date": "20250102"}], "brand_name": "Clopidogrel", "product_id": "72789-469_2abaa65e-cc80-156c-e063-6294a90a44be", "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": "72789-469", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA090540", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}