Package 50268-184-12
Brand: clopidogrel
Generic: clopidogrel bisulfatePackage Facts
Identity
Package NDC
50268-184-12
Digits Only
5026818412
Product NDC
50268-184
Description
20 BLISTER PACK in 1 BOX (50268-184-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-184-11)
Marketing
Marketing Status
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": "486110ba-88b3-80cc-e063-6294a90a28b8", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["749196"], "spl_set_id": ["94a5cdc4-e063-1d46-e053-2995a90a7e15"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX (50268-184-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-184-11)", "package_ndc": "50268-184-12", "marketing_start_date": "20191011"}], "brand_name": "Clopidogrel", "product_id": "50268-184_486110ba-88b3-80cc-e063-6294a90a28b8", "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": "50268-184", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "300 mg/1"}], "application_number": "ANDA204165", "marketing_category": "ANDA", "marketing_start_date": "20191011", "listing_expiration_date": "20271231"}