NDC product
Nexium 24HR
NDC 0573-2451 · Haleon US Holdings LLC
Key facts
| Product NDC | 0573-2451 |
|---|---|
| Proprietary name | Nexium 24HR |
| Nonproprietary name | esomeprazole magnesium |
| Substances | ESOMEPRAZOLE MAGNESIUM TRIHYDRATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Haleon US Holdings LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | NDA |
| Application number | NDA207920 |
| Pharmacologic classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| Marketing start | Feb 6, 2016 |
| Marketing end | May 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