Omeprazole
- Product NDC
- 37012-401
- 11-digit product format
- 370120401
- Labeler code
- 37012
- Product ID
- 37012-401_e5732375-cfb0-431c-b7b8-cacd604efb68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- NDA022032
- Marketing category
- NDA
- Marketing start
- 2015-12-02
- 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 |
|---|
| 37012-401-01 | 37012040101 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (37012-401-01) | | 2015-12-02 | 0000-00-00 | No | No | Current |
| 37012-401-03 | 37012040103 | 3 BOTTLE in 1 CARTON (37012-401-03) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2015-12-02 | 0000-00-00 | No | No | Current |