Esomeprazole Magnesium
- Product NDC
- 42292-009
- 11-digit product format
- 422920009
- Labeler code
- 42292
- Product ID
- 42292-009_d3d2f0c2-9f4f-6c36-e053-2995a90a00c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA078936
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42292-009-16 | 42292000916 | 60 BLISTER PACK in 1 CARTON (42292-009-16) > 1 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (42292-009-01) | 60 blister pack | 2016-06-01 | 0000-00-00 | No | No | Current |