Package 68180-709-06

Brand: rivaroxaban

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 68180-709-06
Digits Only 6818070906
Product NDC 68180-709
Product ID 68180-709_10a06ab0-1eb3-4b5a-8374-65ccbe6ce29e
Description

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

Marketing

Marketing Status
Marketed Since 2025-03-06
Brand rivaroxaban
Generic rivaroxaban
Sample Package No

Linked Drug Pages (1)

RIVAROXABAN ndc-match (0.95)

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"}