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
- 71335-2309_fbf1e034-ee7f-4f4a-84d3-a5ea78fdd363
- Product NDC
- 71335-2309
- Form
- TABLET
- Composition / generic term
- Warfarin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100816
- Source listing expiry
- 20261231
Source-listed ingredients
- WARFARIN SODIUM — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2309-1) · 71335-2309-1
- 14 TABLET in 1 BOTTLE (71335-2309-2) · 71335-2309-2
- 90 TABLET in 1 BOTTLE (71335-2309-3) · 71335-2309-3
- 45 TABLET in 1 BOTTLE (71335-2309-4) · 71335-2309-4
- 50 TABLET in 1 BOTTLE (71335-2309-5) · 71335-2309-5
- 21 TABLET in 1 BOTTLE (71335-2309-6) · 71335-2309-6
- 60 TABLET in 1 BOTTLE (71335-2309-7) · 71335-2309-7
- 20 TABLET in 1 BOTTLE (71335-2309-8) · 71335-2309-8
Source and coverage
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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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