warfarin sodium

Generic: warfarin sodium

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

Drug Facts

Product Profile

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

warfarin sodium 4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0280
Product ID 70518-0280_47e6553f-05b4-8891-e063-6294a90a11c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040616
Listing Expiration 2027-12-31
Marketing Start 2017-03-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180280
Hyphenated Format 70518-0280

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 sodium (source: ndc)
Application Number ANDA040616 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-0280-0)
source: ndc

Packages (1)

70518-0280-0 30 TABLET in 1 BLISTER PACK (70518-0280-0)

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": "47e6553f-05b4-8891-e063-6294a90a11c4", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855324"], "spl_set_id": ["ba65ae56-ca3b-4895-9938-1dde2c3d34bf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0280-0)", "package_ndc": "70518-0280-0", "marketing_start_date": "20170302"}], "brand_name": "Warfarin Sodium", "product_id": "70518-0280_47e6553f-05b4-8891-e063-6294a90a11c4", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "70518-0280", "generic_name": "Warfarin Sodium", "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": "ANDA040616", "marketing_category": "ANDA", "marketing_start_date": "20170302", "listing_expiration_date": "20271231"}