NDC11 62135066990
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 |
|---|---|
| 62135-0669-90 | 62135-0669 |
| 62135-669-90 | 62135-669 |
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 |
|---|---|---|---|---|---|---|
| Quinapril and Hydrochlorothiazide | QUINAPRIL AND HYDROCHLOROTHIAZIDE | Chartwell RX, LLC | 2eae533f-d0af-47e8-a1f2-94bc8cc89b5a | 2023-12-11 | Boxed warning, Warnings, Adverse reactions | 62135-669-90 62135-669 62135066990 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.