NDC11 00135014005
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 |
|---|---|
| 00135-0140-05 | 00135-0140 |
| 00135-0140-5 | 00135-0140 |
| 00135-140-05 | 00135-140 |
| 0135-0140-05 | 0135-0140 |
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 |
|---|---|---|---|---|---|---|
| TUMS EX | CALCIUM CARBONATE | Haleon US Holdings LLC | 593a0494-d669-4bcf-8412-b92645b2d76c | 2024-12-05 | Warnings | 0135-0140-05 0135-0140 00135014005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.