Package 59651-849-18

Brand: rivaroxaban

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 59651-849-18
Digits Only 5965184918
Product NDC 59651-849
Product ID 59651-849_9c3503ce-8ffe-4ff2-a918-700c62f40642
Description

180 TABLET, FILM COATED in 1 BOTTLE (59651-849-18)

Marketing

Marketing Status
Marketed Since 2025-04-10
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": "9c3503ce-8ffe-4ff2-a918-700c62f40642", "openfda": {"nui": ["N0000175635", "N0000175637"], "upc": ["0359651849606"], "unii": ["9NDF7JZ4M3"], "rxcui": ["2059015"], "spl_set_id": ["bcb0e6e7-3006-4d82-8009-c5fddbbfc80d"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (59651-849-18)", "package_ndc": "59651-849-18", "marketing_start_date": "20250410"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59651-849-60)", "package_ndc": "59651-849-60", "marketing_start_date": "20250410"}], "brand_name": "Rivaroxaban", "product_id": "59651-849_9c3503ce-8ffe-4ff2-a918-700c62f40642", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "59651-849", "generic_name": "Rivaroxaban", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rivaroxaban", "active_ingredients": [{"name": "RIVAROXABAN", "strength": "2.5 mg/1"}], "application_number": "ANDA208544", "marketing_category": "ANDA", "marketing_start_date": "20250410", "listing_expiration_date": "20261231"}