NDC product
Omeprazole
NDC 51660-029 · OHM LABORATORIES INC.
Key facts
| Product NDC | 51660-029 |
|---|---|
| Proprietary name | Omeprazole |
| Nonproprietary name | Omeprazole |
| Substances | OMEPRAZOLE |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Labeler | OHM LABORATORIES INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA207891 |
| Pharmacologic classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| Marketing start | Jun 1, 2019 |
| Listing certified through | Dec 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 · Source date: