NDC11 58602081204
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 |
|---|---|
| 58602-0812-04 | 58602-0812 |
| 58602-0812-4 | 58602-0812 |
| 58602-812-04 | 58602-812 |
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 |
|---|---|---|---|---|---|---|
| Cetirizine Hydrochloride (Allergy) | CETIRIZINE HYDROCHLORIDE | Aurohealth LLC | 3cf969e6-6bc9-4dae-ab6a-b24c0fc46b25 | 2026-08-03 | Warnings | 58602-812-04 58602-812 58602081204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.