NDC11 52768010030
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 |
|---|---|
| 52768-0100-30 | 52768-0100 |
| 52768-100-30 | 52768-100 |
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 |
|---|---|---|---|---|---|---|
| AMMONIA N-13 | AMMONIA N-13 | Precision Nuclear LLC | cc430bfd-6940-41ca-bda4-6d29eb4dc1f2 | 2024-12-11 | Warnings, Adverse reactions | 52768-100-30 52768-100 52768010030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.