Esomeprazole Magnesium
- Product NDC
- 59651-805
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA218948
- Marketing category
- ANDA
- Substance
- ESOMEPRAZOLE MAGNESIUM TRIHYDRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 59651-805-30 | 30 GRANULE, DELAYED RELEASE in 1 CARTON (59651-805-30) | 2025-04-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Esomeprazole Magnesium | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | 2025-04-16 | Human Prescription Drug Label | 1 |