NDC11 69729013714
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 |
|---|---|
| 69729-0137-14 | 69729-0137 |
| 69729-137-14 | 69729-137 |
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 |
|---|---|---|---|---|---|---|
| Pentrexcilina Day time | CETIRIZINE HYDROCHLORIDE | OPMX LLC | 26f56cb7-be58-a0c2-e063-6294a90a15fa | 2024-11-15 | Warnings | 69729-137-14 69729-137 69729013714 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.