NDC11 00121090805
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 |
|---|---|
| 00121-0908-05 | 00121-0908 |
| 00121-0908-5 | 00121-0908 |
| 00121-908-05 | 00121-908 |
| 0121-0908-05 | 0121-0908 |
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 |
|---|---|---|---|---|---|---|
| Propranolol Hydrochloride | PROPRANOLOL HYDROCHLORIDE | Pharmaceutical Associates, Inc. | ec5c919b-05d1-45d2-a6e4-ac4ae1101dbb | 2022-06-22 | Warnings, Adverse reactions | 0121-0908-05 0121-0908 00121090805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.