NDC11 44911053201
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 |
|---|---|
| 44911-0532-01 | 44911-0532 |
| 44911-0532-1 | 44911-0532 |
| 44911-532-01 | 44911-532 |
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 |
|---|---|---|---|---|---|---|
| Cardiopar | CONVALLARIA MAJALIS, APOCYNUM CANNABINUM, ARTERIA SUIS, HEART (SUIS), THYROIDINUM (SUIS), ADONIS VERNALIS, CACTUS GRANDIFLORUS, DIGITALIS PURPUREA, LYCOPUS VIRGINICUS | Energique, Inc. | b29cf432-3862-465c-908b-124be5842489 | 2023-06-08 | Warnings | 44911-0532-1 44911-0532 44911053201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.