omeprazole
- Product NDC
- 72288-606
- 11-digit product format
- 722880606
- Labeler code
- 72288
- Product ID
- 72288-606_0cb73d40-2e1f-4197-a2bd-038b2295738f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Amazon.com Services LLC
- Application
- ANDA216096
- Marketing category
- ANDA
- Marketing start
- 2026-04-20
- 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
- 2027-12-31
- 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 |
|---|
| 72288-606-03 | 72288060603 | 3 BOTTLE in 1 CARTON (72288-606-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72288-606-01) | 3 bottle | 2026-04-20 | No | No | Historical |