NDC product
Daypro
NDC 0025-1381 · Pfizer Laboratories Div Pfizer Inc
Key facts
| Product NDC | 0025-1381 |
|---|---|
| Proprietary name | Daypro |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Marketing category | NDA |
| Application number | NDA018841 |
| Marketing start | Oct 29, 1992 |
| Marketing end | Apr 30, 2026 |
| Listing certified through | Apr 30, 2026 |
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: