NDC11 49873040301
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 |
|---|---|
| 49873-0403-01 | 49873-0403 |
| 49873-0403-1 | 49873-0403 |
| 49873-403-01 | 49873-403 |
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 |
|---|---|---|---|---|---|---|
| Inon Ace | MAGNESIUM ALUMINOSILICATE, MAGNESIUM HYDROXIDE | Sato Pharmaceutical Co., Ltd. | a6e4475c-dfac-493c-b98a-21473e3b59d5 | 2023-12-06 | Warnings | 49873-403-01 49873-403 49873040301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.