Omeprazole
- Product NDC
- 51407-287
- 11-digit product format
- 514070287
- Labeler code
- 51407
- Product ID
- 51407-287_3a279e1b-921a-0b97-e063-6394a90a5977
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA212977
- Marketing category
- ANDA
- Marketing start
- 2020-12-10
- Substance
- OMEPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| KG60484QX9 | OMEPRAZOLE | 73590-58-6 | OMEPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-287-30 | 51407028730 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-287-30) | 2023-03-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Omeprazole | Golden State Medical Supply, Inc. | 2025-07-17 | HUMAN PRESCRIPTION DRUG LABEL | 3 |