NDC11 72789017101
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 |
|---|---|
| 72789-0171-01 | 72789-0171 |
| 72789-0171-1 | 72789-0171 |
| 72789-171-01 | 72789-171 |
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. | 039f188c-413a-6e64-e063-6294a90a2972 | 2025-10-20 | Boxed warning, Warnings, Adverse reactions | 72789-171 |
| Lithium Carbonate | LITHIUM CARBONATE | PD-Rx Pharmaceuticals, Inc. | c2635909-7ab2-4c05-9a42-2819702dba63 | 2025-01-20 | Boxed warning, Warnings, Adverse reactions | 72789-171-01 72789-171 72789017101 |