Esomeprazole Magnesium
- Product NDC
- 68071-3735
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078279
- Marketing category
- ANDA
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3735-3 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3735-3) | 2025-04-28 | | No | Historical |
| 68071-3735-6 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3735-6) | 2024-12-04 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Esomeprazole Magnesium | NuCare Pharmaceuticals,Inc. | 2025-04-28 | HUMAN PRESCRIPTION DRUG LABEL | 2 |