Esomeprazole Magnesium
- Product NDC
- 68016-007
- 11-digit product format
- 680160007
- Labeler code
- 68016
- Product ID
- 68016-007_e41d65f1-4c45-422f-b1e2-c5d0dc072934
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Chain Drug Consortium, 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68016-007-14 | 68016000714 | 1 BOTTLE in 1 CARTON (68016-007-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2017-10-16 | 0000-00-00 | No | No | Current |
| 68016-007-42 | 68016000742 | 3 BOTTLE in 1 CARTON (68016-007-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2017-10-16 | 0000-00-00 | No | No | Current |