omeprazole
- Product NDC
- 37012-711
- 11-digit product format
- 370120711
- Labeler code
- 37012
- Product ID
- 37012-711_ba98ab42-6904-4258-904b-87aaa3f3e918
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- omeprazole
- Dosage form
- TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- NDA209400
- Marketing category
- NDA
- Marketing start
- 2018-06-13
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37012-711-55 | 37012071155 | 3 CARTON in 1 CARTON (37012-711-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 3 carton | 2018-06-15 | 0000-00-00 | No | No | Current |
| 37012-711-74 | 37012071174 | 14 BLISTER PACK in 1 CARTON (37012-711-74) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 14 blister pack | 2018-06-13 | 0000-00-00 | No | No | Current |