omeprazole
- Product NDC
- 0904-5834
- 11-digit product format
- 009045834
- Labeler code
- 0904
- Product ID
- 0904-5834_0da1ba3c-6638-4d20-840f-8730e965856f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- NDA022032
- Marketing category
- NDA
- Marketing start
- 2008-02-29
- 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 |
|---|
| 0904-5834-41 | 00904583441 | 14 BLISTER PACK in 1 CARTON (0904-5834-41) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 14 blister pack | 2008-02-29 | 0000-00-00 | No | No | Current |
| 0904-5834-42 | 00904583442 | 3 CARTON in 1 CARTON (0904-5834-42) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 3 carton | 2008-02-29 | 0000-00-00 | No | No | Current |
| 0904-5834-71 | 00904583471 | 2 CARTON in 1 CARTON (0904-5834-71) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 2 carton | 2008-02-29 | 0000-00-00 | No | No | Current |