warfarin sodium
Generic: warfarin
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
warfarin sodium
Generic Name
warfarin
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
warfarin sodium 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2383
Product ID
70518-2383_4a152b72-65fd-e48b-e063-6394a90a1b84
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202202
Listing Expiration
2027-12-31
Marketing Start
2019-10-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182383
Hyphenated Format
70518-2383
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 POUCH in 1 BOX (70518-2383-0) / 1 TABLET in 1 POUCH (70518-2383-1)
- 30 TABLET in 1 BLISTER PACK (70518-2383-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a152b72-65fd-e48b-e063-6394a90a1b84", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855288"], "spl_set_id": ["a4cf3107-5646-4b91-8aae-94548e4409ef"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2383-0) / 1 TABLET in 1 POUCH (70518-2383-1)", "package_ndc": "70518-2383-0", "marketing_start_date": "20191024"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2383-3)", "package_ndc": "70518-2383-3", "marketing_start_date": "20250606"}], "brand_name": "Warfarin Sodium", "product_id": "70518-2383_4a152b72-65fd-e48b-e063-6394a90a1b84", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "70518-2383", "generic_name": "Warfarin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "1 mg/1"}], "application_number": "ANDA202202", "marketing_category": "ANDA", "marketing_start_date": "20191024", "listing_expiration_date": "20271231"}