NDC11 71288043392
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 |
|---|---|
| 71288-0433-92 | 71288-0433 |
| 71288-433-92 | 71288-433 |
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 |
|---|---|---|---|---|---|---|
| Enoxaparin Sodium | ENOXAPARIN SODIUM | Meitheal Pharmaceuticals Inc. | b6fb85ab-1fe5-4dd3-a97f-adbed0674f67 | 2026-01-08 | Boxed warning, Warnings, Adverse reactions | 71288-433-92 71288-433 71288043392 |
| Enoxaparin Sodium | ENOXAPARIN SODIUM | Meitheal Pharmaceuticals Inc. | adbba7bb-fa72-4cec-aa69-13965591a45d | 2025-12-17 | Boxed warning, Warnings, Adverse reactions | 71288-433 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.