NDC product
Omeprazole and sodium bicarbonate
NDC 0363-0732 · Walgreen Company
Key facts
| Product NDC | 0363-0732 |
|---|---|
| Proprietary name | Omeprazole and sodium bicarbonate |
| Nonproprietary name | Omeprazole, sodium bicarbonate |
| Substances | OMEPRAZOLE, SODIUM BICARBONATE |
| Dosage form | CAPSULE, GELATIN COATED |
| Route | ORAL |
| Labeler | Walgreen Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA201361 |
| Pharmacologic classes | Cytochrome P450 2C19 Inhibitors [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Proton Pump Inhibitor [EPC] and 1 more |
| Marketing start | Jul 15, 2016 |
| 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: