ESOMEPRAZOLE MAGNEISUM D/R
- Product NDC
- 61919-868
- 11-digit product format
- 619190868
- Labeler code
- 61919
- Product ID
- 61919-868_8a822b60-49ba-07e4-e053-2995a90aff23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESOMEPRAZOLE MAGNEISUM D/R
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA208333
- Marketing category
- ANDA
- Marketing start
- 2019-06-04
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-868-30 | 61919086830 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-868-30) | 2019-06-04 | 0000-00-00 | No | No | Current |