NDC11 00013104201
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 |
|---|---|
| 00013-1042-01 | 00013-1042 |
| 00013-1042-1 | 00013-1042 |
| 0013-1042-01 | 0013-1042 |
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 |
|---|---|---|---|---|---|---|
| Estring | ESTRADIOL | Pfizer Laboratories Div Pfizer Inc | 110b9865-5a07-4d45-b560-e89947f12600 | 2026-04-23 | Warnings, Adverse reactions | 0013-1042-01 0013-1042 00013104201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.