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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Droptics Performance Eye Drops | NAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOL | Droptics LLC | 20fd6822-a7fd-4593-92bb-0a07260893e2 | 2026-02-09 | Warnings | 6DC9Q167V3 |
| Youmi Alcohol Prep Pad 70 Isopropyl Alcohol | ISOPROPYL ALCOHOL | PT YOUMI MEDIKA INDUSTRI | e3b1a576-a8eb-44bf-8f9c-a49a44a894e8 | 2026-02-09 | Warnings | ND2M416302 |
| EVERLIT CARE PRODUCTS PREP PAD | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | 77a60360-8bb5-43e9-b7e4-f71d2d488c44 | 2026-02-09 | Warnings | ND2M416302 |
| Everlit Care Products Sting Relief | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | adfab206-b7de-4f6a-a864-edd946ea743d | 2026-02-09 | Warnings | ND2M416302 |
| Mold, Yeast and Dust | ADRENALINUM, ARSENICUM IODATUM, ASPERGILLUS FLAVUS, ASPERGILLUS FUMIGATUS, ASPERGILLUS GLAUCUS, ASPERGILLUS NIDULANS, ASPERGILLUS NIGER, CANDIDA ALBICANS, DERMATOPHAGOIDES FARINAE, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR PLUMBEUS, NATRUM SULPHURICUM, PENICILLIUM DIGITATUM, PENICILLIUM ROQUEFORTII, SACCHAROMYCES CEREVISIAE, SILICEA | NaturalCare | 32afa0f0-bca5-4246-bc2e-decd757fcf9d | 2026-02-09 | Warnings | ETJ7Z6XBU4 |
| Alcohol | ISOPROPYL ALCOHOL | A-S Medication Solutions | 6b8834be-0235-4f7c-8d52-c2f6aa2d3049 | 2026-02-08 | Warnings | ND2M416302 |
| members mark esomeprazole magnesium | ESOMEPRAZOLE | Sam's West Inc | 87913038-4b90-40a0-bce5-2d368bd5758c | 2026-02-07 | Warnings | 606726 |
| Hampton Sun SPF 50 Mineral | ZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00% | S&C Hampton Sun LLC | d6c33436-042e-44e8-8b55-98be6e246879 | 2026-02-06 | Warnings | 15FIX9V2JP |
| SHISEIDO WASO COLOR-SMART DAY MOISTURIZER | OCTINOXATE, TITANIUM DIOXIDE | Shiseido Americas Corporation | f291f077-1c72-48fc-bb19-c20bdeaaa596 | 2026-02-06 | Warnings | 15FIX9V2JP |
| Hand Sanitizer | ALCOHOL | Retail Business Services, LLC | 8ba8176f-ddbd-48d7-bb62-74a499ea667c | 2026-02-06 | Warnings, Adverse reactions | 3K9958V90M |
| Advanced Hand Sanitizer | ETHYL ALCOHOL | Retail Business Services, LLC | 135ae232-3be4-4bbe-98fd-65eef3a675ad | 2026-02-06 | Warnings, Adverse reactions | 3K9958V90M |
| SHISEIDO WASO COLOR-SMART DAY MOISTURIZER | OCTINOXATE, TITANIUM DIOXIDE | Shiseido Americas Corporation | 54f63dd8-e77f-42e4-a6d3-61ab7beecf50 | 2026-02-06 | Warnings | 15FIX9V2JP |
| Advanced Hand Sanitizer | ALCOHOL | Salado Sales Inc. | 2869f574-e74c-492c-b3fa-b256b468746b | 2026-02-06 | Warnings, Adverse reactions | 3K9958V90M |
| SEYTU Body Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | c411e9a6-b2ea-446b-a886-b92c61736e6c | 2026-02-05 | Warnings | 15FIX9V2JP |
| SEYTU Facial Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | 96fd37fb-c3ff-413f-b2c8-50754f320ecc | 2026-02-05 | Warnings | 15FIX9V2JP |
| 70% Rubbing | ISOPROPYL ALCOHOL | Walgreens Co. | 6ad37d18-5c19-4b5f-8313-edd430f84fb0 | 2026-02-05 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Walgreens Co. | 1473e6e4-dc5f-43d9-a249-111a181e3f76 | 2026-02-05 | Warnings, Adverse reactions | ND2M416302 |
| ForPro Premium Sterile Antiseptic Isopropyl Alcohol Pads | ISOPROPYL ALCOHOL | Tng workdwide | 6cc2ccae-b288-473e-a736-0974c96dbb89 | 2026-02-05 | Warnings | ND2M416302 |
| Hand Sanitizer Cherry Pop | ALCOHOL | Scent Theory Products LLC | 4a18b475-fd3b-10a3-e063-6294a90a4f47 | 2026-02-05 | Warnings | 3K9958V90M |
| Hand Sanitizer Ocean Splash | ALCOHOL | Scent Theory Products LLC | 4a18d7b2-94ca-7924-e063-6394a90af3d1 | 2026-02-05 | Warnings | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.