Package 72189-405-71

Brand: warfarin sodium

Generic: warfarin sodium
NDC Package

Package Facts

Identity

Package NDC 72189-405-71
Digits Only 7218940571
Product NDC 72189-405
Description

100 TABLET in 1 BOTTLE (72189-405-71)

Marketing

Marketing Status
Marketed Since 2022-12-15
Brand warfarin sodium
Generic warfarin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4ced46-ac01-014b-e063-6394a90a5a5d", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855324"], "spl_set_id": ["efded00a-22b9-1da7-e053-2995a90a58ca"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-405-71)", "package_ndc": "72189-405-71", "marketing_start_date": "20221215"}], "brand_name": "WARFARIN SODIUM", "product_id": "72189-405_2c4ced46-ac01-014b-e063-6394a90a5a5d", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72189-405", "generic_name": "WARFARIN SODIUM", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "WARFARIN SODIUM", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "4 mg/1"}], "application_number": "ANDA202202", "marketing_category": "ANDA", "marketing_start_date": "20221215", "listing_expiration_date": "20261231"}