NDC11 62332014891
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 |
|---|---|
| 62332-0148-91 | 62332-0148 |
| 62332-148-91 | 62332-148 |
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 | Alembic Pharmaceuticals Inc. | a1e2f942-2bc0-4afd-91ad-6c4cab38c8f0 | 2024-12-12 | Boxed warning, Adverse reactions | 62332-148-91 62332-148 62332014891 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.