Omeprazole
- Product NDC
- 50090-4829
- 11-digit product format
- 500904829
- Labeler code
- 50090
- Product ID
- 50090-4829_0720ca37-d87a-4387-be48-f21117a949e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075576
- Marketing category
- ANDA
- Marketing start
- 2009-01-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4829-0 | Omeprazole | 32 in 1 BOTTLE, UNIT-DOSE | CAPSULE, DELAYED RELEASE | 32 | | 3 |
| 50090-4829-0 | Omeprazole | 1 in 1 BLISTER PACK | CAPSULE, DELAYED RELEASE | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4829 | OMEPRAZOLE CAPSULE, DELAYED RELEASE [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210615_97f62c65-ef06-4cc6-8887-46c81266a80a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4829-0 | 50090482900 | 32 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (50090-4829-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 32 blister pack | 2020-01-08 | 0000-00-00 | No | No | Current |