NDC11 00173072200
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 |
|---|---|
| 00173-0722-0 | 00173-0722 |
| 00173-0722-00 | 00173-0722 |
| 00173-722-00 | 00173-722 |
| 0173-0722-00 | 0173-0722 |
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 |
|---|---|---|---|---|---|---|
| WELLBUTRIN SR | BUPROPION HYDROCHLORIDE | GlaxoSmithKline LLC | cbc8c074-f080-4489-a5ae-207b5fadeba3 | 2025-11-05 | Boxed warning, Warnings, Adverse reactions | 0173-0722-00 0173-0722 00173072200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.