warfarin sodium

Generic: warfarin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2395
Product ID 70518-2395_4a16ce66-f7bf-0dbb-e063-6394a90ac907
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202202
Listing Expiration 2027-12-31
Marketing Start 2019-10-28

Pharmacologic Class

Classes
vitamin k antagonist [epc] vitamin k inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182395
Hyphenated Format 70518-2395

Supplemental Identifiers

RxCUI
855324
UNII
6153CWM0CL

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name warfarin sodium (source: ndc)
Generic Name warfarin (source: ndc)
Application Number ANDA202202 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-2395-0) / 1 TABLET in 1 POUCH (70518-2395-1)
source: ndc

Packages (1)

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

Ingredients (1)

warfarin sodium (4 mg/1)

Linked Drug Pages (1)

Warfarin Sodium ndc-match (0.9)

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"}