NDC11 16714011002
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 |
|---|---|
| 16714-0110-02 | 16714-0110 |
| 16714-0110-2 | 16714-0110 |
| 16714-110-02 | 16714-110 |
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 |
|---|---|---|---|---|---|---|
| Hydroxychloroquine sulfate | HYDROXYCHLOROQUINE SULFATE | Northstar Rx LLC. | 29ba0172-7ca3-4122-af1b-f0da522318cb | 2023-12-22 | Warnings, Adverse reactions | 16714-110-02 16714-110 16714011002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.