NDC11 35573010749
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 |
|---|---|
| 35573-0107-49 | 35573-0107 |
| 35573-107-49 | 35573-107 |
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 |
|---|---|---|---|---|---|---|
| BETAMETHASONE DIPROPIONATE | BETAMETHASONE DIPROPIONATE | Burel Pharmaceuticals, LLC | c8bda9a8-4dec-4084-84e5-4b4623390bd8 | 2024-12-04 | Warnings, Adverse reactions | 35573-107-49 35573-107 35573010749 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.