Package 46708-240-51

Brand: rivaroxaban

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 46708-240-51
Digits Only 4670824051
Product NDC 46708-240
Product ID 46708-240_4b61dc52-0593-4ef0-8246-a82ff6972842
Description

1 KIT in 1 CARTON (46708-240-51) * 42 TABLET, FILM COATED in 1 BLISTER PACK * 9 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-05-14
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 
{"spl_id": "4b61dc52-0593-4ef0-8246-a82ff6972842", "openfda": {"nui": ["N0000175635", "N0000175637"], "unii": ["9NDF7JZ4M3"], "rxcui": ["1114198", "1232082", "1232086", "1549682", "2059015"], "spl_set_id": ["5524f30f-789d-4f5c-8f7c-d03a475b6d34"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (46708-240-51)  *  42 TABLET, FILM COATED in 1 BLISTER PACK *  9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "46708-240-51", "marketing_start_date": "20250514"}], "brand_name": "RIVAROXABAN", "product_id": "46708-240_4b61dc52-0593-4ef0-8246-a82ff6972842", "dosage_form": "KIT", "product_ndc": "46708-240", "generic_name": "RIVAROXABAN", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RIVAROXABAN", "application_number": "ANDA210301", "marketing_category": "ANDA", "marketing_start_date": "20250514", "listing_expiration_date": "20261231"}