NDC11 70748033204
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 |
|---|---|
| 70748-0332-04 | 70748-0332 |
| 70748-0332-4 | 70748-0332 |
| 70748-332-04 | 70748-332 |
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 |
|---|---|---|---|---|---|---|
| PREDNISOLONE ACETATE | PREDNISOLONE ACETATE | Lupin Pharmaceuticals, Inc. | 75fbeab1-ce8d-4999-a875-472174be5cc6 | 2025-10-13 | Warnings, Adverse reactions | 70748-332-04 70748-332 70748033204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.