Over-the-counter drug · ANDA
Omeprazole delayed release (omeprazole 20mg) NDC 49483-731
Omeprazole magnesium 20 mg/1 · Tablet, Delayed release · Oral · TIME CAP LABORATORIES, INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 49483-731-41 | 49483073141 | 3 BOTTLE in 1 CARTON (49483-731-41) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (49483-731-45)Marketed from Dec 15, 2025 |
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 delayed release
- Generic name (nonproprietary)
- omeprazole 20mg
- Active ingredients
- Omeprazole magnesium — 20 mg/1
- Dosage form
- Tablet, Delayed release
- Route
- Oral
- Labeler
- TIME CAP LABORATORIES, INC.
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 218829
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
- Identifiers
- Product ID 49483-731_442e2a90-4ac6-8adf-e063-6394a90a6fc2SPL ID 442e2a90-4ac6-8adf-e063-6394a90a6fc2SPL set ID 40906798-cd84-fbd0-e063-6294a90a1d29RxCUI 402014UNII 426QFE7XLKUPC 0349483731415
- 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
N449483073141followed by a unit qualifier and the quantityPackage 49483-0731-41. 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)
Uses 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 218829
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 20 mg | Omeprazole magnesium 20 mg/1 | Tablet, Delayed releaseOral | MARKSANS PHARMA LIMITED | 25000-094 |
| Omeprazole 20 mg | Omeprazole magnesium 20 mg/1 | Tablet, Delayed releaseOral | MARKSANS PHARMA LIMITED | 25000-091 |
| Omeprazole Delayed-Releaseomeprazole | Omeprazole magnesium 20 mg/1 | Tablet, Delayed releaseOral | H-E-B | 37808-569 |
| 24 HOUR Omeprazoleomeprazole 20 mg | Omeprazole magnesium 20 mg/1 | Tablet, Delayed releaseOral | Grocery Outlet, Inc. | 85828-731 |