NDC product
Gleevec
NDC 0078-0401 · Novartis Pharmaceuticals Corporation
Key facts
| Product NDC | 0078-0401 |
|---|---|
| Proprietary name | Gleevec |
| Nonproprietary name | imatinib mesylate |
| Substances | IMATINIB MESYLATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Novartis Pharmaceuticals Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA021588 |
| Pharmacologic classes | Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Kinase Inhibitor [EPC] |
| Marketing start | May 15, 2001 |
| Listing certified through | Dec 31, 2027 |
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: