Package 50090-3639-0

Brand: xarelto

Generic: rivaroxaban
NDC Package

Package Facts

Identity

Package NDC 50090-3639-0
Digits Only 5009036390
Product NDC 50090-3639
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-3639-0)

Marketing

Marketing Status
Marketed Since 2018-10-08
Brand xarelto
Generic rivaroxaban
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e5d5aa2f-de19-4bad-a5c4-1136fe148975", "openfda": {"nui": ["N0000175635", "N0000175637"], "unii": ["9NDF7JZ4M3"], "rxcui": ["1232086", "1232088"], "spl_set_id": ["3e95389b-0a93-4560-98c5-02637fb2600f"], "pharm_class_epc": ["Factor Xa Inhibitor [EPC]"], "pharm_class_moa": ["Factor Xa Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-3639-0)", "package_ndc": "50090-3639-0", "marketing_start_date": "20181008"}], "brand_name": "XARELTO", "product_id": "50090-3639_e5d5aa2f-de19-4bad-a5c4-1136fe148975", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Factor Xa Inhibitor [EPC]", "Factor Xa Inhibitors [MoA]"], "product_ndc": "50090-3639", "generic_name": "rivaroxaban", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "XARELTO", "active_ingredients": [{"name": "RIVAROXABAN", "strength": "20 mg/1"}], "application_number": "NDA022406", "marketing_category": "NDA", "marketing_start_date": "20111105", "listing_expiration_date": "20261231"}