NDC product
PROVENGE
NDC 30237-8900 · Dendreon Pharmaceuticals LLC
Key facts
| Product NDC | 30237-8900 |
|---|---|
| Proprietary name | PROVENGE |
| Nonproprietary name | sipuleucel-T |
| Substances | SIPULEUCEL-T |
| Dosage form | INJECTION |
| Route | INTRAVENOUS |
| Labeler | Dendreon Pharmaceuticals LLC |
| Product type | CELLULAR THERAPY |
| Marketing category | BLA |
| Application number | BLA125197 |
| Pharmacologic classes | Autologous Cellular Immunotherapy [EPC], Cell-mediated Immunity [PE], Cells, Cultured, Autologous [EXT], Leukocytes and 1 more |
| Marketing start | Apr 29, 2010 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: