NDC product
PNEUMOVAX 23
NDC 0006-4739 · Merck Sharp & Dohme LLC
Key facts
| Product NDC | 0006-4739 |
|---|---|
| Proprietary name | PNEUMOVAX 23 |
| Labeler | Merck Sharp & Dohme LLC |
| Marketing category | BLA |
| Application number | BLA101094 |
| Marketing start | Jul 7, 1983 |
| Marketing end | May 16, 2015 |
| Listing certified through | May 16, 2015 |
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: