ESOMEPRAZOLE MAGNESIUM
- Product NDC
- 72189-318
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESOMEPRAZOLE MAGNESIUM
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA211977
- Marketing category
- ANDA
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-318-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-318-30) | 2022-01-19 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Esomeprazole | Direct Rx | 2025-01-21 | HUMAN PRESCRIPTION DRUG LABEL | 4 |