NDC product
Omeprazole 20 mg
NDC 25000-091 · MARKSANS PHARMA LIMITED
Key facts
| Product NDC | 25000-091 |
|---|---|
| Proprietary name | Omeprazole 20 mg |
| Nonproprietary name | Omeprazole 20 mg |
| Substances | OMEPRAZOLE MAGNESIUM |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Labeler | MARKSANS PHARMA LIMITED |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA218829 |
| Pharmacologic classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| Marketing start | Aug 12, 2025 |
| Listing certified through | Dec 31, 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: