NDC11 75053000301
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 |
|---|---|
| 75053-0003-01 | 75053-0003 |
| 75053-0003-1 | 75053-0003 |
| 75053-003-01 | 75053-003 |
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 |
|---|---|---|---|---|---|---|
| Celltem | CARBO VEGETABILIS, ANILINUM, RADIUM BROMATUM, MILLEFOLIUM, MEDULLA OSSIS SUIS, RNA, DNA, METHYLENE BLUE, ABROTANUM, CALCAREA OXALICA, CONIUM MACULATUM, EUPHORBIA COROLLATA, EUPHORBIUM OFFICINARUM | Nucleic Products, LLC | cd6670f1-d910-4228-ad8c-0bbe173e3a8c | 2025-03-20 | Warnings | 75053-0003-1 75053-0003 75053000301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.