Package 70518-2395-0

Brand: warfarin sodium

Generic: warfarin
NDC Package

Package Facts

Identity

Package NDC 70518-2395-0
Digits Only 7051823950
Product NDC 70518-2395
Description

100 POUCH in 1 BOX (70518-2395-0) / 1 TABLET in 1 POUCH (70518-2395-1)

Marketing

Marketing Status
Marketed Since 2019-10-28
Brand warfarin sodium
Generic warfarin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a16ce66-f7bf-0dbb-e063-6394a90ac907", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855324"], "spl_set_id": ["545ec40d-2db1-4581-b3ec-ce195e5f5400"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2395-0)  / 1 TABLET in 1 POUCH (70518-2395-1)", "package_ndc": "70518-2395-0", "marketing_start_date": "20191028"}], "brand_name": "Warfarin Sodium", "product_id": "70518-2395_4a16ce66-f7bf-0dbb-e063-6394a90ac907", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "70518-2395", "generic_name": "Warfarin", "labeler_name": "REMEDYREPACK INC.", "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": "20191028", "listing_expiration_date": "20271231"}