NDC11 62135096990
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 |
|---|---|
| 62135-0969-90 | 62135-0969 |
| 62135-969-90 | 62135-969 |
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 |
|---|---|---|---|---|---|---|
| Moexipril Hydrochloride | MOEXIPRIL HYDROCHLORIDE | Chartwell RX, LLC | 5c24072c-9769-4cb5-b8da-bf814d21391d | 2025-03-10 | Boxed warning, Warnings, Adverse reactions | 62135-969-90 62135-969 62135096990 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.