NDC11 00049151501
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 |
|---|---|
| 00049-1515-01 | 00049-1515 |
| 00049-1515-1 | 00049-1515 |
| 0049-1515-01 | 0049-1515 |
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 |
|---|---|---|---|---|---|---|
| UNASYN | AMPICILLIN SODIUM AND SULBACTAM SODIUM | Roerig | 12eeb72a-403d-41be-bae4-4cb930862884 | 2026-07-09 | Warnings, Adverse reactions | 0049-1515-01 0049-1515 00049151501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.