rivaroxaban

Generic: rivaroxaban

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rivaroxaban
Generic Name rivaroxaban
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

rivaroxaban 2.5 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-709
Product ID 68180-709_10a06ab0-1eb3-4b5a-8374-65ccbe6ce29e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208555
Listing Expiration 2026-12-31
Marketing Start 2025-03-06

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 68180709
Hyphenated Format 68180-709

Supplemental Identifiers

RxCUI
2059015
UPC
0368180709060
UNII
9NDF7JZ4M3
NUI
N0000175635 N0000175637

Packaging Origin

Original Packager
true

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 rivaroxaban (source: ndc)
Generic Name rivaroxaban (source: ndc)
Application Number ANDA208555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68180-709-06)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68180-709-09)
source: ndc

Packages (2)

68180-709-06 30 TABLET, FILM COATED in 1 BOTTLE (68180-709-06) 68180-709-09 90 TABLET, FILM COATED in 1 BOTTLE (68180-709-09)

Ingredients (1)

rivaroxaban (2.5 mg/1)

Linked Drug Pages (1)

RIVAROXABAN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10a06ab0-1eb3-4b5a-8374-65ccbe6ce29e", "openfda": {"nui": ["N0000175635", "N0000175637"], "upc": ["0368180709060"], "unii": ["9NDF7JZ4M3"], "rxcui": ["2059015"], "spl_set_id": ["702fed3e-ae25-49ba-98cc-562e0e244214"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68180-709-06)", "package_ndc": "68180-709-06", "marketing_start_date": "20250306"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68180-709-09)", "package_ndc": "68180-709-09", "marketing_start_date": "20250306"}], "brand_name": "RIVAROXABAN", "product_id": "68180-709_10a06ab0-1eb3-4b5a-8374-65ccbe6ce29e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "68180-709", "generic_name": "RIVAROXABAN", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RIVAROXABAN", "active_ingredients": [{"name": "RIVAROXABAN", "strength": "2.5 mg/1"}], "application_number": "ANDA208555", "marketing_category": "ANDA", "marketing_start_date": "20250306", "listing_expiration_date": "20261231"}