Package 70518-4462-0

Brand: eliquis

Generic: apixaban
NDC Package

Package Facts

Identity

Package NDC 70518-4462-0
Digits Only 7051844620
Product NDC 70518-4462
Product ID 70518-4462_3d82588d-1d34-1c57-e063-6294a90af174
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4462-0)

Marketing

Marketing Status
Marketed Since 2025-08-29
Brand eliquis
Generic apixaban
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d82588d-1d34-1c57-e063-6294a90af174", "openfda": {"nui": ["N0000175637", "N0000175635"], "unii": ["3Z9Y7UWC1J"], "rxcui": ["1364445", "1364447"], "spl_set_id": ["7be1f4c1-bb2f-4ded-ae9a-515d2a22f93e"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4462-0)", "package_ndc": "70518-4462-0", "marketing_start_date": "20250829"}], "brand_name": "ELIQUIS", "product_id": "70518-4462_3d82588d-1d34-1c57-e063-6294a90af174", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "70518-4462", "generic_name": "apixaban", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ELIQUIS", "active_ingredients": [{"name": "APIXABAN", "strength": "5 mg/1"}], "application_number": "NDA202155", "marketing_category": "NDA", "marketing_start_date": "20250829", "listing_expiration_date": "20261231"}