NDC11 42708001230
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 |
|---|---|
| 42708-0012-30 | 42708-0012 |
| 42708-012-30 | 42708-012 |
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 |
|---|---|---|---|---|---|---|
| Atenolol | ATENOLOL | QPharma, Inc. | 70d7a585-7a46-4eac-b2b5-2ac5b98d9882 | 2025-12-05 | Boxed warning, Warnings, Adverse reactions | 42708-012-30 42708-012 42708001230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.