Package 72189-210-71

Brand: warfarin sodium

Generic: warfarin sodium
NDC Package

Package Facts

Identity

Package NDC 72189-210-71
Digits Only 7218921071
Product NDC 72189-210
Description

100 TABLET in 1 BOTTLE (72189-210-71)

Marketing

Marketing Status
Marketed Since 2021-05-04
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": "2be9877c-0b1d-23b4-e063-6394a90af68f", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855296"], "spl_set_id": ["c186d1ff-64dd-bfcb-e053-2a95a90af800"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-210-71)", "package_ndc": "72189-210-71", "marketing_start_date": "20210504"}], "brand_name": "WARFARIN SODIUM", "product_id": "72189-210_2be9877c-0b1d-23b4-e063-6394a90af68f", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72189-210", "generic_name": "WARFARIN SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "WARFARIN SODIUM", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA090935", "marketing_category": "ANDA", "marketing_start_date": "20210504", "listing_expiration_date": "20261231"}