NDC11 51991097401
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 |
|---|---|
| 51991-0974-01 | 51991-0974 |
| 51991-0974-1 | 51991-0974 |
| 51991-974-01 | 51991-974 |
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 |
|---|---|---|---|---|---|---|
| Penicillamine | PENICILLAMINE | Breckenridge Pharmaceutical, Inc. | 1320f46b-e243-4e93-b9c9-ad8eb7828de5 | 2026-08-14 | Boxed warning, Warnings, Adverse reactions | 51991-974-01 51991-974 51991097401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.