NDC 65862-784-10 - Esomeprazole Magnesium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 65862-784
- Requested NDC
- 65862-784-10
- Package NDCs from labels
- 65862-784-30, 65862-784-90, 65862-784-01, 65862-784-99, 65862-784-10, 65862-784-78
- Manufacturer
- Aurobindo Pharma Limited
- Effective date
- 2025-03-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Esomeprazole Magnesium - Aurobindo Pharma Limited | Aurobindo Pharma Limited | 2025-03-26 | Human Prescription Drug Label |
| Esomeprazole Magnesium - NCS HealthCare of KY, LLC dba Vangard Labs | NCS HealthCare of KY, LLC dba Vangard Labs | 2024-09-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Esomeprazole Magnesium - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2020-05-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Esomeprazole Magnesium - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2018-01-04 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65862-784-01 | Esomeprazole Magnesium | 100 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 100 | 15 | |
| 65862-784-10 | Esomeprazole Magnesium | 10 in 1 BLISTER PACK | CAPSULE, DELAYED RELEASE | 10 | 15 | |
| 65862-784-30 | Esomeprazole Magnesium | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | 15 | |
| 65862-784-78 | Esomeprazole Magnesium | 10 in 1 CARTON | CAPSULE, DELAYED RELEASE | 10 | 15 | |
| 65862-784-90 | Esomeprazole Magnesium | 90 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 90 | 15 | |
| 65862-784-99 | Esomeprazole Magnesium | 1000 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 1000 | 15 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65862-784-30 | EA - Each | 65862-784 | 87b9131b-9e7a-48ca-820b-83be58b67c91 | 1 | 2016-12-07 |
| 65862-784-90 | EA - Each | 65862-784 | 74b427bf-b382-462b-840f-177111a01147 | 1 | 2016-12-07 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.