Omeprazole
- Product NDC
- 50090-2901
- 11-digit product format
- 500902901
- Labeler code
- 50090
- Product ID
- 50090-2901_a8110f69-2275-4b9e-bd86-5ebf9ca04103
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075757
- Marketing category
- ANDA
- Marketing start
- 2003-01-28
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-2901-0 | EA - Each | 50090-2901 | 84702db0-2617-48bc-a6d0-bf72362558d8 | 1 | 2019-04-11 |
| 50090-2901-2 | EA - Each | 50090-2901 | 7286f5e9-c377-4122-9bc5-648010264fa2 | 1 | 2019-04-11 |
| 50090-2901-3 | EA - Each | 50090-2901 | 63f98fc1-6ed2-4be0-83d7-0189d99fae3a | 1 | 2018-09-05 |
| 50090-2901-4 | EA - Each | 50090-2901 | cb63155d-f000-4277-9a3f-f7da4ca4829e | 1 | 2019-04-11 |
| 50090-2901-5 | EA - Each | 50090-2901 | 9093d78e-54ae-4788-975e-f6a96a97c05c | 1 | 2019-04-11 |
| 50090-2901-6 | EA - Each | 50090-2901 | 154d1e95-2594-4d84-ac5d-bf034856bed1 | 1 | 2019-04-11 |
| 50090-2901-7 | EA - Each | 50090-2901 | 3dcd75b7-36b1-4664-8a04-1b3a136deb2d | 1 | 2019-04-11 |
| 50090-2901-8 | EA - Each | 50090-2901 | 3f9199b7-e30f-49de-86ab-7658059c2495 | 1 | 2019-04-11 |