Esomeprazole magnesium
- Product NDC
- 68071-4888
- 11-digit product format
- 680714888
- Labeler code
- 68071
- Product ID
- 68071-4888_bb90b075-654c-0760-e053-2a95a90af72e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208333
- Marketing category
- ANDA
- Marketing start
- 2017-10-20
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4888-6 | 68071488806 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-4888-6) | 2019-05-09 | 0000-00-00 | No | No | Current |