NDC11 16714052701
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 |
|---|---|
| 16714-0527-01 | 16714-0527 |
| 16714-0527-1 | 16714-0527 |
| 16714-527-01 | 16714-527 |
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 |
|---|---|---|---|---|---|---|
| Ipratropium Bromide | IPRATROPIUM BROMIDE | NORTHSTAR RX LLC | e592b6b5-038a-dbe8-457e-76e88a0f194a | 2026-02-27 | Warnings, Adverse reactions | 16714-527-01 16714-527 16714052701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.