OMEPRAZOLE
- Product NDC
- 51407-130
- 11-digit product format
- 514070130
- Labeler code
- 51407
- Product ID
- 51407-130_b60c6517-b7e9-1f90-e053-2995a90a63ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OMEPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA203481
- Marketing category
- ANDA
- Marketing start
- 2017-07-03
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-130-01 | 51407013001 | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-130-01) | 2018-10-15 | 0000-00-00 | No | No | Current |
| 51407-130-05 | 51407013005 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-130-05) | 2018-10-15 | 0000-00-00 | No | No | Current |
| 51407-130-30 | 51407013030 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-130-30) | 2018-10-15 | 0000-00-00 | No | No | Current |
| 51407-130-90 | 51407013090 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-130-90) | 2018-10-15 | 0000-00-00 | No | No | Current |