United States · FDA National Drug Code directory

Warfarin Sodium

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70518-2383_5564b633-eaed-d561-e063-6394a90aa6ab
Product NDC
70518-2383
Form
TABLET
Composition / generic term
Warfarin
Labeler
REMEDYREPACK INC.
Marketing category
ANDA
Marketing start / end (source format)
20191024
Source listing expiry
20271231

Source-listed ingredients

  • WARFARIN SODIUM — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 POUCH in 1 BOX (70518-2383-0) / 1 TABLET in 1 POUCH (70518-2383-1) · 70518-2383-0
  • 30 TABLET in 1 BLISTER PACK (70518-2383-3) · 70518-2383-3
  • 30 TABLET in 1 BLISTER PACK (70518-2383-4) · 70518-2383-4

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Warfarin Sodium — United States | Molindra Medicines