NDC product
SIVEXTRO
NDC 67919-041 · Merck Sharp & Dohme LLC
Key facts
| Product NDC | 67919-041 |
|---|---|
| Proprietary name | SIVEXTRO |
| Nonproprietary name | tedizolid phosphate |
| Substances | TEDIZOLID PHOSPHATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Merck Sharp & Dohme LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA205435 |
| Pharmacologic classes | Breast Cancer Resistance Protein Inhibitors [MoA], Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS] |
| Marketing start | Jun 20, 2014 |
| 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: