NDC11 00363201022
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 |
|---|---|
| 00363-2010-22 | 00363-2010 |
| 0363-2010-22 | 0363-2010 |
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 |
|---|---|---|---|---|---|---|
| Allergy Relief D | LORATADINE, PSEUDOEPHEDRINE SULFATE | Walgreen Company | 9952e0fb-b20e-4f9c-8be7-aa286e271fee | 2026-02-28 | Warnings | 0363-2010-22 0363-2010 00363201022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.