Esomeprazole magnesium
- Product NDC
- 0186-0384
- 11-digit product format
- 001860384
- Labeler code
- 0186
- Product ID
- 0186-0384_1c4578d8-b561-4f13-9175-7fbf2eec64b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- NDA021153
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-10-01
- Marketing end
- 2022-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0186-0384-30 | 00186038430 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0384-30) | 2017-10-01 | 2022-08-31 | No | No | Current |
| 0186-0384-90 | 00186038490 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0384-90) | 2017-10-01 | 2022-05-31 | No | No | Current |