eliquis

Generic: apixaban

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name eliquis
Generic Name apixaban
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

apixaban 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4462
Product ID 70518-4462_3d82588d-1d34-1c57-e063-6294a90af174
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA202155
Listing Expiration 2026-12-31
Marketing Start 2025-08-29

Pharmacologic Class

Established (EPC)
factor xa inhibitor [epc]
Mechanism of Action
factor xa inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184462
Hyphenated Format 70518-4462

Supplemental Identifiers

RxCUI
1364445 1364447
UNII
3Z9Y7UWC1J
NUI
N0000175637 N0000175635

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name eliquis (source: ndc)
Generic Name apixaban (source: ndc)
Application Number NDA202155 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4462-0)
source: ndc

Packages (1)

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

Ingredients (1)

apixaban (5 mg/1)

Linked Drug Pages (1)

ELIQUIS ndc-match (0.9)

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"}