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 | Type |
|---|---|---|---|
| Warfarin Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-06-29 | HUMAN 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Warfarin Sodium | WARFARIN | Aphena Pharma Solutions - Tennessee, LLC | 91f24482-d4cb-4a09-a97e-64f6e49071ee | 2020-08-03 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | Proficient Rx LP | 73048ed9-242f-4f86-a8db-9c7547daa01d | 2020-05-01 | Boxed warning, Warnings, Adverse reactions | 855296 855312 6153CWM0CL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.