NDC11 00013010130
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 |
|---|---|
| 00013-0101-30 | 00013-0101 |
| 00013-101-30 | 00013-101 |
| 0013-0101-30 | 0013-0101 |
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 |
|---|---|---|---|---|---|---|
| Azulfidine | SULFASALAZINE | Pfizer Laboratories Div Pfizer Inc | ddbe69f3-bd55-45f3-a64f-f60226c744c4 | 2026-05-29 | Warnings, Adverse reactions | 0013-0101-30 0013-0101 00013010130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.