NDC11 47335099102
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 |
|---|---|
| 47335-0991-02 | 47335-0991 |
| 47335-0991-2 | 47335-0991 |
| 47335-991-02 | 47335-991 |
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 |
|---|---|---|---|---|---|---|
| Glatiramer Acetate | GLATIRAMER ACETATE | Sun Pharmaceutical Industries, Inc. | dfacc3e2-5c91-41de-a377-873276a5cf67 | 2025-02-18 | Boxed warning, Warnings, Adverse reactions | 47335-991-02 47335-991 47335099102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.