NDC11 51672210201
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 |
|---|---|
| 51672-2102-01 | 51672-2102 |
| 51672-2102-1 | 51672-2102 |
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 |
|---|---|---|---|---|---|---|
| Childrens Cetirizine Hydrochloride Sugar Free Grape | CETIRIZINE HYDROCHLORIDE | Sun Pharmaceutical Industries, Inc. | 54d72d7a-1f5b-4b36-bf76-ab7aef6243ab | 2025-07-02 | Warnings | 51672-2102-1 51672-2102 51672210201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.