Package 60505-6256-6

Brand: rivaroxaban

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 60505-6256-6
Digits Only 6050562566
Product NDC 60505-6256
Product ID 60505-6256_14ee2935-fe14-6d8a-8305-c410bc494c48
Description

60 TABLET, FILM COATED in 1 BOTTLE (60505-6256-6)

Marketing

Marketing Status
Marketed Since 2025-05-02
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": "14ee2935-fe14-6d8a-8305-c410bc494c48", "openfda": {"nui": ["N0000175635", "N0000175637"], "upc": ["0360505625666", "0360505625659"], "unii": ["9NDF7JZ4M3"], "rxcui": ["2059015"], "spl_set_id": ["e98f6d83-5172-97a1-ee41-5d7d1d8ba2fd"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60505-6256-5)", "package_ndc": "60505-6256-5", "marketing_start_date": "20250502"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (60505-6256-6)", "package_ndc": "60505-6256-6", "marketing_start_date": "20250502"}], "brand_name": "Rivaroxaban", "product_id": "60505-6256_14ee2935-fe14-6d8a-8305-c410bc494c48", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "60505-6256", "generic_name": "Rivaroxaban", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rivaroxaban", "active_ingredients": [{"name": "RIVAROXABAN", "strength": "2.5 mg/1"}], "application_number": "ANDA217810", "marketing_category": "ANDA", "marketing_start_date": "20250502", "listing_expiration_date": "20261231"}