Esomeprazole Magnesium
- Product NDC
- 59726-912
- 11-digit product format
- 597260912
- Labeler code
- 59726
- Product ID
- 59726-912_141be1c1-d85e-42ed-9d04-c7a8b1885307
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA209716
- Marketing category
- ANDA
- Marketing start
- 2020-01-31
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-912 | ESOMEPRAZOLE MAGNESIUM CAPSULE, DELAYED RELEASE [P & L DEVELOPMENT, LLC] | 2 | Legacy NDC | 20230419_777e1cf2-2cda-4c47-9fac-10f670d279ed.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-912-14 | 59726091214 | 1 BOTTLE in 1 CARTON (59726-912-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-01-31 | 0000-00-00 | No | No | Current |