NDC11 00472001304
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 |
|---|---|
| 00472-0013-04 | 00472-0013 |
| 00472-0013-4 | 00472-0013 |
| 00472-013-04 | 00472-013 |
| 0472-0013-04 | 0472-0013 |
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 |
|---|---|---|---|---|---|---|
| Griseofulvin | GRISEOFULVIN | Actavis Pharma, Inc. | af318d5d-cc39-4a63-a590-b87c50f2694f | 2023-09-30 | Warnings, Adverse reactions | 0472-0013-04 0472-0013 00472001304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.