NDC product
CRIXIVAN
NDC 0006-0573 · Merck Sharp & Dohme LLC
Key facts
| Product NDC | 0006-0573 |
|---|---|
| Proprietary name | CRIXIVAN |
| Labeler | Merck Sharp & Dohme LLC |
| Marketing category | NDA |
| Application number | NDA020685 |
| Marketing start | Mar 13, 1996 |
| Marketing end | Oct 24, 2021 |
| Listing certified through | Oct 24, 2021 |
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: