NDC11 51662123502
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 |
|---|---|
| 51662-1235-02 | 51662-1235 |
| 51662-1235-2 | 51662-1235 |
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 |
|---|---|---|---|---|---|---|
| 50% MAGNESIUM SULFATE | 50% MAGNESIUM SULFATE | HF Acquisition Co. LLC, DBA Health First | 7446d09b-10fe-7765-e053-2a91aa0a56a8 | 2026-06-11 | Warnings, Adverse reactions | 51662-1235-2 51662-1235 51662123502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.