NDC11 24979001012
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 24979-0010-12 | 24979-0010 |
| 24979-010-12 | 24979-010 |
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 |
|---|---|---|---|---|---|---|
| Nifedipine | NIFEDIPINE | Upsher-Smith Laboratories, LLC | 160271a8-7922-2107-e054-00144ff88e88 | 2026-01-19 | Warnings, Adverse reactions | 24979-010-12 24979-010 24979001012 |
| Nifedipine | NIFEDIPINE | Upsher-Smith Laboratories, LLC | 3bf4282f-b063-4d35-8ef0-6f48b98e9deb | 2026-01-19 | Warnings, Adverse reactions | 24979-010 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.