NDC product
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · Takeda Pharmaceutical Company Limited
NDC 11532-3002 · Takeda Pharmaceutical Company Limited
Key facts
| Product NDC | 11532-3002 |
|---|---|
| Nonproprietary name | VEDOLIZUMAB |
| Substances | VEDOLIZUMAB |
| Dosage form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Labeler | Takeda Pharmaceutical Company Limited |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| Marketing start | May 20, 2014 |
| 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: