NDC11 49884011701
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 |
|---|---|
| 49884-0117-01 | 49884-0117 |
| 49884-0117-1 | 49884-0117 |
| 49884-117-01 | 49884-117 |
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 |
|---|---|---|---|---|---|---|
| Amiloride Hydrochloride | AMILORIDE HYDROCHLORIDE | Par Health USA, LLC | e0cc2d44-436a-47e8-a890-589882fff4c4 | 2026-07-28 | Warnings, Adverse reactions | 49884-117-01 49884-117 49884011701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.