NDC11 83027000501
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 |
|---|---|
| 83027-0005-01 | 83027-0005 |
| 83027-0005-1 | 83027-0005 |
| 83027-005-01 | 83027-005 |
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 |
|---|---|---|---|---|---|---|
| Femmepap | THUJA OCCIDENTALIS, NITRICUM ACIDUM, CAUSTICUM, SABINA, X-RAY, ANTIMONIUM SULPHURATUM, HUMAN PAPILLOMA NOSODE, ADENOVIREN NOSODE | Nutritional Specialties, Inc. | 68e8f960-f8d2-4083-8681-51d6d2acd8bc | 2024-07-25 | Warnings | 83027-0005-1 83027-0005 83027000501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.