Package 72162-2230-0

Brand: warfarin sodium

Generic: warfarin sodium
NDC Package

Package Facts

Identity

Package NDC 72162-2230-0
Digits Only 7216222300
Product NDC 72162-2230
Product ID 72162-2230_4a06b3c4-8a13-4eb1-862d-856885e27641
Description

1000 TABLET in 1 BOTTLE (72162-2230-0)

Marketing

Marketing Status
Marketed Since 2024-01-26
Brand warfarin sodium
Generic warfarin sodium
Sample Package No

Linked Drug Pages (1)

Warfarin Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a06b3c4-8a13-4eb1-862d-856885e27641", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855318"], "spl_set_id": ["f827bb9a-6afd-4d0c-a7ca-bdef0667be52"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2230-0)", "package_ndc": "72162-2230-0", "marketing_start_date": "20240126"}], "brand_name": "Warfarin Sodium", "product_id": "72162-2230_4a06b3c4-8a13-4eb1-862d-856885e27641", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72162-2230", "generic_name": "warfarin sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "3 mg/1"}], "application_number": "ANDA090935", "marketing_category": "ANDA", "marketing_start_date": "20111111", "listing_expiration_date": "20261231"}