NDC11 00093081301
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 |
|---|---|
| 00093-0813-01 | 00093-0813 |
| 00093-0813-1 | 00093-0813 |
| 00093-813-01 | 00093-813 |
| 0093-0813-01 | 0093-0813 |
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 |
|---|---|---|---|---|---|---|
| Nortriptyline Hydrochloride | NORTRIPTYLINE HYDROCHLORIDE | Teva Pharmaceuticals USA, Inc. | b58d473a-b19f-4d2a-b1ae-dd398d7a29e1 | 2025-09-30 | Boxed warning, Warnings, Adverse reactions | 0093-0813-01 0093-0813 00093081301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.