NDC11 00093593898
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 |
|---|---|
| 00093-5938-98 | 00093-5938 |
| 0093-5938-98 | 0093-5938 |
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 |
|---|---|---|---|---|---|---|
| Lanthanum carbonate | LANTHANUM CARBONATE | Teva Pharmaceuticals USA, Inc. | e4b88992-ecb0-455b-b68c-5c4e6d3cf521 | 2025-01-30 | Warnings, Adverse reactions | 0093-5938-98 0093-5938 00093593898 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.