warfarin sodium

Generic: warfarin sodium

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin sodium
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 4 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7358
Product ID 68788-7358_510d1a24-563c-4e63-807f-c031fe44e39f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090935
Listing Expiration 2026-12-31
Marketing Start 2011-11-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887358
Hyphenated Format 68788-7358

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 ANDA090935 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7358-1)
  • 30 TABLET in 1 BOTTLE (68788-7358-3)
  • 60 TABLET in 1 BOTTLE (68788-7358-6)
  • 90 TABLET in 1 BOTTLE (68788-7358-9)
source: ndc

Packages (4)

68788-7358-1 100 TABLET in 1 BOTTLE (68788-7358-1) 68788-7358-3 30 TABLET in 1 BOTTLE (68788-7358-3) 68788-7358-6 60 TABLET in 1 BOTTLE (68788-7358-6) 68788-7358-9 90 TABLET in 1 BOTTLE (68788-7358-9)

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": "510d1a24-563c-4e63-807f-c031fe44e39f", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855324"], "spl_set_id": ["b2bf6749-3d9a-49e3-8f6b-f7db80d236b8"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7358-1)", "package_ndc": "68788-7358-1", "marketing_start_date": "20191001"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7358-3)", "package_ndc": "68788-7358-3", "marketing_start_date": "20191001"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7358-6)", "package_ndc": "68788-7358-6", "marketing_start_date": "20191001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7358-9)", "package_ndc": "68788-7358-9", "marketing_start_date": "20191001"}], "brand_name": "Warfarin Sodium", "product_id": "68788-7358_510d1a24-563c-4e63-807f-c031fe44e39f", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "68788-7358", "generic_name": "warfarin sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "4 mg/1"}], "application_number": "ANDA090935", "marketing_category": "ANDA", "marketing_start_date": "20111111", "listing_expiration_date": "20261231"}