Over-the-counter drug · ANDA
Omeprazole NDC 79903-305
Omeprazole 20 mg/1 · Tablet, Delayed release · Oral · Walmart Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 79903-305-28 | 79903030528 | 2 BOTTLE in 1 CARTON (79903-305-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79903-305-14)Marketed from Feb 3, 2025 | |
| 79903-305-41 | 79903030541 | 1 BOTTLE in 1 CARTON (79903-305-41) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79903-305-14)Marketed from Mar 28, 2026 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Omeprazole
- Generic name (nonproprietary)
- omeprazole
- Active ingredients
- Omeprazole — 20 mg/1
- Dosage form
- Tablet, Delayed release
- Route
- Oral
- Labeler
- Walmart Inc.
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 207740
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
- Identifiers
- Product ID 79903-305_cd2683cb-42a1-cb9f-6dd4-a1464ddb3afdSPL ID cd2683cb-42a1-cb9f-6dd4-a1464ddb3afdSPL set ID 5168ccd9-31b4-3a49-85b9-4f202cd99f6bRxCUI 402014UNII KG60484QX9
- Pharmacologic class
- Proton Pump Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N479903030528followed by a unit qualifier and the quantityPackage 79903-0305-28. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 207740
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | AMERISOURCEBERGEN DRUG CORPORATION | 46122-739 |
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | Walgreens Company | 0363-1607 |
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | Chain Drug Marketing Association INC | 83324-141 |
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | Dr. Reddys Laboratories Inc | 43598-286 |
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | BluePoint Laboratories | 68001-441 |
| Omeprazole | Omeprazole 20 mg/1 | Tablet, Delayed releaseOral | Dr. Reddys Laboratories Inc | 43598-841 |