NDC11 43853004001
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 |
|---|---|
| 43853-0040-01 | 43853-0040 |
| 43853-0040-1 | 43853-0040 |
| 43853-040-01 | 43853-040 |
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 |
|---|---|---|---|---|---|---|
| THYROPRO | CALCAREA IODATA, FERRUM IODATUM, KALI IODATUM, SPONGIA TOSTA, FUCUS VESICULOSUS, THYROIDINUM, GLANDULA SUPRARENALIS, HYPOPHYSIS, LAPIS ALBUS, HYDROFLUORICUM ACIDUM | ProBlen | e69b797a-678f-4173-9c6c-97b7ba436fbe | 2022-11-30 | Warnings | 43853-0040-1 43853-0040 43853004001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.