eliquis

Generic: apixaban

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name eliquis
Generic Name apixaban
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

apixaban 5 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-662
Product ID 71610-662_2ceefa5f-84de-f3d9-e063-6394a90a6dc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA202155
Listing Expiration 2026-12-31
Marketing Start 2012-12-28

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 71610662
Hyphenated Format 71610-662

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
  • 9000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-09)
  • 3000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-18)
  • 1800 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-42)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-80)
source: ndc

Packages (4)

71610-662-09 9000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-09) 71610-662-18 3000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-18) 71610-662-42 1800 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-42) 71610-662-80 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-80)

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": "2ceefa5f-84de-f3d9-e063-6394a90a6dc5", "openfda": {"nui": ["N0000175637", "N0000175635"], "unii": ["3Z9Y7UWC1J"], "rxcui": ["1364445", "1364447"], "spl_set_id": ["41a133ef-e461-48ad-8221-b735bdd0ec25"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-09)", "package_ndc": "71610-662-09", "marketing_start_date": "20220908"}, {"sample": false, "description": "3000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-18)", "package_ndc": "71610-662-18", "marketing_start_date": "20221017"}, {"sample": false, "description": "1800 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-42)", "package_ndc": "71610-662-42", "marketing_start_date": "20250127"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-662-80)", "package_ndc": "71610-662-80", "marketing_start_date": "20230201"}], "brand_name": "ELIQUIS", "product_id": "71610-662_2ceefa5f-84de-f3d9-e063-6394a90a6dc5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "71610-662", "generic_name": "apixaban", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20121228", "listing_expiration_date": "20261231"}