NDC11 68462022301
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 |
|---|---|
| 68462-0223-01 | 68462-0223 |
| 68462-0223-1 | 68462-0223 |
| 68462-223-01 | 68462-223 |
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 | Glenmark Pharmaceuticals Inc., USA | 1b65d27e-5086-4a87-8387-c49f3d060978 | 2026-01-30 | Boxed warning, Warnings, Adverse reactions | 68462-223-01 68462-223 68462022301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.