NDC product
Daypro Alta
NDC 0025-5500 · Pfizer Laboratories Div Pfizer Inc
Key facts
| Product NDC | 0025-5500 |
|---|---|
| Proprietary name | Daypro Alta |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Marketing category | NDA |
| Application number | NDA020776 |
| Marketing start | Oct 17, 2002 |
| Marketing end | Aug 10, 2007 |
| Listing certified through | Aug 10, 2007 |
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: