NDC11 83027000301
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 |
|---|---|
| 83027-0003-01 | 83027-0003 |
| 83027-0003-1 | 83027-0003 |
| 83027-003-01 | 83027-003 |
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 |
|---|---|---|---|---|---|---|
| Sciatic Formula | KALI IODATUM, RUTA GRAVEOLENS, AMMONIUM MURIATICUM, BELLADONNA, GNAPHALIUM POLYCEPHALUM, COLOCYNTHIS, ACONITUM NAPELLUS, NUX VOMICA, ARSENICUM ALBUM | Nutritional Specialties, Inc. | 76c5cb3f-0f1b-47b8-a492-592ff440c7da | 2023-02-22 | Warnings | 83027-0003-1 83027-0003 83027000301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.