Package 70518-2380-0

Brand: warfarin sodium

Generic: warfarin
NDC Package

Package Facts

Identity

Package NDC 70518-2380-0
Digits Only 7051823800
Product NDC 70518-2380
Product ID 70518-2380_4a14fc67-5718-ab7a-e063-6394a90ae5ec
Description

100 POUCH in 1 BOX (70518-2380-0) / 1 TABLET in 1 POUCH (70518-2380-1)

Marketing

Marketing Status
Marketed Since 2019-10-23
Brand warfarin sodium
Generic warfarin
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a14fc67-5718-ab7a-e063-6394a90ae5ec", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855318"], "spl_set_id": ["884cdbf6-0a52-4126-8e14-b0d7c9367e33"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2380-0)  / 1 TABLET in 1 POUCH (70518-2380-1)", "package_ndc": "70518-2380-0", "marketing_start_date": "20191023"}], "brand_name": "Warfarin Sodium", "product_id": "70518-2380_4a14fc67-5718-ab7a-e063-6394a90ae5ec", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "70518-2380", "generic_name": "Warfarin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "3 mg/1"}], "application_number": "ANDA202202", "marketing_category": "ANDA", "marketing_start_date": "20191023", "listing_expiration_date": "20271231"}