NDC11 57664002397
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 |
|---|---|
| 57664-0023-97 | 57664-0023 |
| 57664-023-97 | 57664-023 |
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 |
|---|---|---|---|---|---|---|
| Isotretinoin | ISOTRETINOIN | Sun Pharmaceutical Industries, Inc. | b44200ba-6672-4ea7-b151-7caec3f53c9c | 2024-01-10 | Boxed warning, Warnings, Adverse reactions | 57664-023-97 57664-023 57664002397 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.