NDC11 42023024301
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 |
|---|---|
| 42023-0243-01 | 42023-0243 |
| 42023-0243-1 | 42023-0243 |
| 42023-243-01 | 42023-243 |
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 |
|---|---|---|---|---|---|---|
| EPHEDRINE SULFATE | EPHEDRINE SULFATE | Par Health USA, LLC | a247857e-ba7b-4a37-b132-4ba9b0d1c4d1 | 2023-05-31 | Warnings, Adverse reactions | 42023-243 |
| EPHEDRINE SULFATE | EPHEDRINE SULFATE | Par Health USA, LLC | 2c203482-8a04-40fc-93d2-74b30dec7742 | 2022-04-30 | Warnings, Adverse reactions | 42023-243-01 42023-243 42023024301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.