omeprazole
- Product NDC
- 30142-474
- 11-digit product format
- 301420474
- Labeler code
- 30142
- Product ID
- 30142-474_90aa0006-a47e-4058-bff3-5fb2d7bef8f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- NDA022032
- Marketing category
- NDA
- Marketing start
- 2025-05-05
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- omeprazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OMEPRAZOLE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | KG60484QX9 |
| Rxcui | 402014 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30142-474-01 | omeprazole | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | | 2 |
| 30142-474-01 | omeprazole | 14 in 1 BOTTLE | TABLET, DELAYED RELEASE | 14 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 30142-474-01 | 30142047401 | 1 BOTTLE in 1 CARTON (30142-474-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2025-05-05 | No | No | Current |