Esomeprazole Magnesium
- Product NDC
- 16714-735
- 11-digit product format
- 167140735
- Labeler code
- 16714
- Product ID
- 16714-735_26990f16-e3d3-4491-a99d-1cc5411f2e86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA205606
- Marketing category
- ANDA
- Marketing start
- 2017-08-14
- Marketing end
- 2021-12-01
- Substance
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE
- 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
- 0000-00-00
- 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 |
|---|
| 16714-735-01 | 16714073501 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-735-01) | 2017-08-14 | 2021-12-01 | No | No | Current |
| 16714-735-02 | 16714073502 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-735-02) | 2017-08-14 | 2021-12-01 | No | No | Current |