NDC11 47335099201
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 |
|---|---|
| 47335-0992-01 | 47335-0992 |
| 47335-0992-1 | 47335-0992 |
| 47335-992-01 | 47335-992 |
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 |
|---|---|---|---|---|---|---|
| MAGNESIUM SULFATE | MAGNESIUM SULFATE HEPTAHYDRATE | Sun Pharmaceutical Industries, Inc. | efadcb55-f935-4c60-b2e2-0a76b9194b50 | 2026-01-29 | Warnings, Adverse reactions | 47335-992-01 47335-992 47335099201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.