NDC product
BOSULIF
NDC 0069-0135 · Pfizer Laboratories Div Pfizer Inc
Key facts
| Product NDC | 0069-0135 |
|---|---|
| Proprietary name | BOSULIF |
| Nonproprietary name | Bosutinib |
| Substances | BOSUTINIB MONOHYDRATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA203341 |
| Pharmacologic classes | Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC] |
| Marketing start | Sep 4, 2012 |
| 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: