NDC11 72789017301
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 |
|---|---|
| 72789-0173-01 | 72789-0173 |
| 72789-0173-1 | 72789-0173 |
| 72789-173-01 | 72789-173 |
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 |
|---|---|---|---|---|---|---|
| Lithium Carbonate | LITHIUM CARBONATE | PD-Rx Pharmaceuticals, Inc. | c4973d87-d014-42f4-ba13-ae628ca1a451 | 2025-10-08 | Boxed warning, Warnings, Adverse reactions | 72789-173-01 72789-173 72789017301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.