NDC product
Xalkori
NDC 0069-0251 · Pfizer Laboratories Div Pfizer Inc
Key facts
| Product NDC | 0069-0251 |
|---|---|
| Proprietary name | Xalkori |
| Nonproprietary name | CRIZOTINIB |
| Substances | CRIZOTINIB |
| Dosage form | CAPSULE, COATED PELLETS |
| Route | ORAL |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA217581 |
| Pharmacologic classes | Cytochrome P450 2B6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], Organic Cation Transporter 1 Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA] and 1 more |
| Marketing start | Nov 20, 2023 |
| 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: