Package 51672-4228-9

{"route": ["ORAL"], "spl_id": "44213d0b-ca52-c6ac-e063-6394a90afd03", "openfda": {"nui": ["N0000175635", "N0000175637"], "unii": ["9NDF7JZ4M3"], "rxcui": ["2059015"], "spl_set_id": ["925a9a11-ae5b-405c-96d2-b1be4b85bf71"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (51672-4228-4)", "package_ndc": "51672-4228-4", "marketing_start_date": "20251015"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (51672-4228-9)", "package_ndc": "51672-4228-9", "marketing_start_date": "20251015"}], "brand_name": "Rivaroxaban", "product_id": "51672-4228_44213d0b-ca52-c6ac-e063-6394a90afd03", "dosage_form": "TABLET, COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "51672-4228", "generic_name": "Rivaroxaban", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rivaroxaban", "active_ingredients": [{"name": "RIVAROXABAN", "strength": "2.5 mg/1"}], "application_number": "ANDA208557", "marketing_category": "ANDA", "marketing_start_date": "20251015", "listing_expiration_date": "20261231"}