NDC11 42291049601
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 |
|---|---|
| 42291-0496-01 | 42291-0496 |
| 42291-0496-1 | 42291-0496 |
| 42291-496-01 | 42291-496 |
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 ER | LITHIUM CARBONATE | AvKARE | d8ddff4d-2b77-a8f2-e053-2a95a90a5fc0 | 2026-01-14 | Boxed warning, Warnings, Adverse reactions | 42291-496-01 42291-496 42291049601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.