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
- 70518-2382_55134e91-612d-b109-e063-6394a90ad96f
- Product NDC
- 70518-2382
- Form
- TABLET
- Composition / generic term
- Warfarin
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191023
- Source listing expiry
- 20271231
Source-listed ingredients
- WARFARIN SODIUM — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 POUCH in 1 BOX (70518-2382-0) / 1 TABLET in 1 POUCH (70518-2382-1) · 70518-2382-0
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-2382-2) · 70518-2382-2
- 30 TABLET in 1 BLISTER PACK (70518-2382-4) · 70518-2382-4
- 30 TABLET in 1 BLISTER PACK (70518-2382-5) · 70518-2382-5
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.
Browse United States records →