Omeprazole
- Product NDC
- 50090-7018
- 11-digit product format
- 500907018
- Labeler code
- 50090
- Product ID
- 50090-7018_b30a1877-ae69-4694-8cd7-cc1f910136fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091352
- Marketing category
- ANDA
- Marketing start
- 2012-11-23
- 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 |
|---|
| 50090-7018-0 | 50090701800 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-0) | 2024-01-04 | No | No | Historical |
| 50090-7018-2 | 50090701802 | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-2) | 2024-01-04 | No | No | Historical |
| 50090-7018-3 | 50090701803 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-3) | 2024-01-04 | No | No | Historical |
| 50090-7018-4 | 50090701804 | 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-4) | 2024-01-04 | No | No | Historical |
| 50090-7018-5 | 50090701805 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-5) | 2024-01-04 | No | No | Historical |
| 50090-7018-6 | 50090701806 | 200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-6) | 2024-01-04 | No | No | Historical |
| 50090-7018-7 | 50090701807 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-7) | 2024-01-04 | No | No | Historical |
| 50090-7018-8 | 50090701808 | 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-8) | 2024-01-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Omeprazole | A-S Medication Solutions | 2024-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 8 |