Esomeprazole Magnesium
- Product NDC
- 55910-016
- 11-digit product format
- 559100016
- Labeler code
- 55910
- Product ID
- 55910-016_dc8b4dc8-7621-43dd-a61d-5f768d5bcd38
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Dolgencorp, LLC
- Application
- ANDA209339
- Marketing category
- ANDA
- Marketing start
- 2017-10-16
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55910-016-03 | 55910001603 | 2 BOTTLE in 1 CARTON (55910-016-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2017-10-16 | 0000-00-00 | No | No | Current |
| 55910-016-04 | 55910001604 | 3 BOTTLE in 1 CARTON (55910-016-04) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2017-10-16 | 0000-00-00 | No | No | Current |
| 55910-016-74 | 55910001674 | 1 BOTTLE in 1 CARTON (55910-016-74) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2017-10-16 | 0000-00-00 | No | No | Current |