NDC11 24338013610
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 |
|---|---|
| 24338-0136-10 | 24338-0136 |
| 24338-136-10 | 24338-136 |
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 |
|---|---|---|---|---|---|---|
| E.E.S 400 | ERYTHROMYCIN ETHYLSUCCINATE | Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) | b455bbdb-a3f1-470f-aa5f-ed83ac2e228d | 2023-12-16 | Warnings, Adverse reactions | 24338-136-10 24338-136 24338013610 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.