NDC product
Temozolomide
NDC 0781-2692 · Sandoz Inc.
Key facts
| Product NDC | 0781-2692 |
|---|---|
| Proprietary name | Temozolomide |
| Labeler | Sandoz Inc. |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA021029 |
| Marketing start | Aug 12, 2013 |
| Marketing end | Sep 12, 2022 |
| Listing certified through | Sep 12, 2022 |
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: