Package 50090-6451-0

Brand: eliquis

Generic: apixaban
NDC Package

Package Facts

Identity

Package NDC 50090-6451-0
Digits Only 5009064510
Product NDC 50090-6451
Description

60 TABLET, FILM COATED in 1 BOTTLE (50090-6451-0)

Marketing

Marketing Status
Marketed Since 2023-04-24
Brand eliquis
Generic apixaban
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "696a119e-a84a-47ba-97cf-39cd5ea5dcd3", "openfda": {"nui": ["N0000175637", "N0000175635"], "unii": ["3Z9Y7UWC1J"], "rxcui": ["1364435", "1364441"], "spl_set_id": ["fd383ae7-1e34-44ef-b8f1-ca6906dfbcef"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6451-0)", "package_ndc": "50090-6451-0", "marketing_start_date": "20230424"}], "brand_name": "ELIQUIS", "product_id": "50090-6451_696a119e-a84a-47ba-97cf-39cd5ea5dcd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "50090-6451", "generic_name": "apixaban", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ELIQUIS", "active_ingredients": [{"name": "APIXABAN", "strength": "2.5 mg/1"}], "application_number": "NDA202155", "marketing_category": "NDA", "marketing_start_date": "20121228", "listing_expiration_date": "20261231"}