NDC11 00132011324
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 |
|---|---|
| 00132-0113-24 | 00132-0113 |
| 00132-113-24 | 00132-113 |
| 0132-0113-24 | 0132-0113 |
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 |
|---|---|---|---|---|---|---|
| Pedia-Lax | DOCUSATE SODIUM | C.B. Fleet Company, Inc. | 0e908bea-ebab-44e7-919c-90002e6f5d42 | 2024-10-01 | Warnings | 0132-0113-24 0132-0113 00132011324 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.