Package 68071-5277-9

Brand: clopidogrel bisulfate

Generic: clopidogrel bisulfate
NDC Package

Package Facts

Identity

Package NDC 68071-5277-9
Digits Only 6807152779
Product NDC 68071-5277
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)

Marketing

Marketing Status
Marketed Since 2020-06-10
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": "1d7904db-ccb2-b88e-e063-6294a90ac568", "openfda": {"upc": ["0368071527797"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["a7bf847d-43e9-166e-e053-2995a90a239e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)", "package_ndc": "68071-5277-9", "marketing_start_date": "20200610"}], "brand_name": "Clopidogrel bisulfate", "product_id": "68071-5277_1d7904db-ccb2-b88e-e063-6294a90ac568", "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": "68071-5277", "generic_name": "Clopidogrel bisulfate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel bisulfate", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA204165", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}