Package 62332-240-51

Brand: rivaroxaban

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 62332-240-51
Digits Only 6233224051
Product NDC 62332-240
Description

1 KIT in 1 CARTON (62332-240-51) * 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)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "43438909-74d8-4b11-b947-00d06de77c88", "openfda": {"nui": ["N0000175635", "N0000175637"], "upc": ["0362332347308", "0362332348305", "0362332683604", "0362332346301"], "unii": ["9NDF7JZ4M3"], "rxcui": ["1114198", "1232082", "1232086", "1549682", "2059015"], "spl_set_id": ["e62f23c6-89f2-4179-95dc-5732401b3f93"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (62332-240-51)  *  42 TABLET, FILM COATED in 1 BLISTER PACK *  9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62332-240-51", "marketing_start_date": "20250514"}], "brand_name": "RIVAROXABAN", "product_id": "62332-240_43438909-74d8-4b11-b947-00d06de77c88", "dosage_form": "KIT", "product_ndc": "62332-240", "generic_name": "RIVAROXABAN", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RIVAROXABAN", "application_number": "ANDA210301", "marketing_category": "ANDA", "marketing_start_date": "20250514", "listing_expiration_date": "20261231"}