NDC11 73302045601
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 |
|---|---|
| 73302-0456-01 | 73302-0456 |
| 73302-0456-1 | 73302-0456 |
| 73302-456-01 | 73302-456 |
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 |
|---|---|---|---|---|---|---|
| Ella | ULIPRISTAL ACETATE | PMI Branded Pharmaceuticals, Inc. | 2bf93d23-cddd-4613-9066-5b5fa090404b | 2026-07-20 | Warnings, Adverse reactions | 73302-456-01 73302-456 73302045601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.