NDC11 83027014101
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 |
|---|---|
| 83027-0141-01 | 83027-0141 |
| 83027-0141-1 | 83027-0141 |
| 83027-141-01 | 83027-141 |
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, ANTIMONIUM SULPHURATUM RUBRUM, HUMAN PAPILLOMA NOSODE, X-RAY, ADENOVIREN NOSODE | Nutritional Specialties, Inc. | 69121519-3b95-4811-87f1-3f8a0d532f69 | 2024-07-25 | Warnings | 83027-0141-1 83027-0141 83027014101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.