NDC 70518-2816-01 - Warfarin Sodium

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70518-2816
Requested NDC
70518-2816-01
Package NDCs from labels
70518-2816-1, 70518-2816-0, 70518-2816-2, 70518-2816-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-06-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Warfarin Sodium - REMEDYREPACK INC.REMEDYREPACK INC.2026-06-29HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 5 of 5 · 82 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Warfarin SodiumWARFARINAphena Pharma Solutions - Tennessee, LLC91f24482-d4cb-4a09-a97e-64f6e49071ee2020-08-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 855332
unii: 6153CWM0CL
Warfarin SodiumWARFARIN SODIUMProficient Rx LP73048ed9-242f-4f86-a8db-9c7547daa01d2020-05-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 855296
rxcui: 855312
unii: 6153CWM0CL

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.