Omeprazole
- Product NDC
- 67296-2183
- 11-digit product format
- 672962183
- Labeler code
- 67296
- Product ID
- 67296-2183_44f5aafa-b7be-b398-e063-6394a90ab9f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA207891
- Marketing category
- ANDA
- Marketing start
- 2019-06-01
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2183-8 | 67296218308 | 2 BOTTLE in 1 CARTON (67296-2183-8) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2019-06-01 | No | No | Historical |