NDC11 60290004204
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 |
|---|---|
| 60290-0042-04 | 60290-0042 |
| 60290-0042-4 | 60290-0042 |
| 60290-042-04 | 60290-042 |
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 |
|---|---|---|---|---|---|---|
| Atorvastatin calcium | ATORVASTATIN CALCIUM | Umedica Laboratories USA Inc. | 5a7594ca-30be-4350-827f-ef745a2a7e18 | 2026-01-30 | Warnings, Adverse reactions | 60290-042-04 60290-042 60290004204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.