Package 70518-1898-0

Brand: clopidogrel

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 70518-1898-0
Digits Only 7051818980
Product NDC 70518-1898
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1898-0)

Marketing

Marketing Status
Marketed Since 2019-02-22
Brand clopidogrel
Generic clopidogrel bisulfate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4987afa4-e527-4ae3-e063-6394a90aa694", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["3e2539c1-a6ad-4d60-944c-c2e7aa70ce45"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1898-0)", "package_ndc": "70518-1898-0", "marketing_start_date": "20190222"}], "brand_name": "Clopidogrel", "product_id": "70518-1898_4987afa4-e527-4ae3-e063-6394a90aa694", "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": "70518-1898", "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": "ANDA090540", "marketing_category": "ANDA", "marketing_start_date": "20190222", "listing_expiration_date": "20271231"}