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 table
LabelManufacturerEffective dateType
Esomeprazole Magnesium - Aurobindo Pharma LimitedAurobindo Pharma Limited2025-03-26Human Prescription Drug Label
Esomeprazole Magnesium - NCS HealthCare of KY, LLC dba Vangard LabsNCS HealthCare of KY, LLC dba Vangard Labs2024-09-16HUMAN PRESCRIPTION DRUG LABEL
Esomeprazole Magnesium - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2020-05-14HUMAN PRESCRIPTION DRUG LABEL
Esomeprazole Magnesium - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2018-01-04HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65862-784-01Esomeprazole Magnesium100 in 1 BOTTLECAPSULE, DELAYED RELEASE10015
65862-784-10Esomeprazole Magnesium10 in 1 BLISTER PACKCAPSULE, DELAYED RELEASE1015
65862-784-30Esomeprazole Magnesium30 in 1 BOTTLECAPSULE, DELAYED RELEASE3015
65862-784-78Esomeprazole Magnesium10 in 1 CARTONCAPSULE, DELAYED RELEASE1015
65862-784-90Esomeprazole Magnesium90 in 1 BOTTLECAPSULE, DELAYED RELEASE9015
65862-784-99Esomeprazole Magnesium1000 in 1 BOTTLECAPSULE, DELAYED RELEASE100015

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65862-784ESOMEPRAZOLE MAGNESIUM CAPSULE, DELAYED RELEASE [AUROBINDO PHARMA LIMITED]15Current NDC, Legacy NDC, 6 package rows20250417_f4ae091d-9b74-4a0e-ac68-057effd91e17.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-784-30EA - Each65862-78487b9131b-9e7a-48ca-820b-83be58b67c9112016-12-07
65862-784-90EA - Each65862-78474b427bf-b382-462b-840f-177111a0114712016-12-07

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.

Matched openFDA labels page 27 of 328 · 6,557 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Anti Bacterial Hand Gel Disney Princess TianaALCOHOLBath & Body Works, Inc.552fc414-20c6-dad6-e063-6394a90a44e82026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Disney Princess Snow WhiteALCOHOLBath & Body Works, Inc.552fbc11-171d-fe10-e063-6294a90ac2362026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Fresh Cut LilacsALCOHOLBath & Body Works, Inc.552fc40c-47f6-a2bc-e063-6394a90a1ba62026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Disney Princess RapunzelALCOHOLBath & Body Works, Inc.552fc8da-e386-0dc5-e063-6294a90a9c0c2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Disney Princess AuroraALCOHOLBath & Body Works, Inc.552fc40c-47f8-a2bc-e063-6394a90a1ba62026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Peach BelliniALCOHOLBath & Body Works, Inc.552fd963-5f09-0acc-e063-6294a90a2c142026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Fresh RainfallALCOHOLBath & Body Works, Inc.552faf37-a7ff-df22-e063-6394a90a47cb2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Sparkling WatermelonALCOHOLBath & Body Works, Inc.552fe62e-5e14-1fed-e063-6294a90a489e2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Warm Vanilla SugarALCOHOLBath & Body Works, Inc.552fbc11-1720-fe10-e063-6294a90ac2362026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Champagne ToastALCOHOLBath & Body Works, Inc.552fc4da-f24c-e88a-e063-6394a90ae2ab2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Eucalyptus MintALCOHOLBath & Body Works, Inc.552fc8da-e38a-0dc5-e063-6294a90a9c0c2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Mango Papaya ParadiseALCOHOLBath & Body Works, Inc.552fe73b-38de-0c49-e063-6394a90a64742026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Moisturizing Hand Sanitizer Strawberry Peach SunsetALCOHOLBath & Body Works, Inc.552fe62e-5e13-1fed-e063-6294a90a489e2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel White Tea and SageALCOHOLBath & Body Works, Inc.552fed13-f320-27bc-e063-6294a90ae1312026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Pink Peach BlossomALCOHOLBath & Body Works, Inc.552feb22-c355-0572-e063-6394a90afa8c2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Sunshine and LemonsALCOHOLBath & Body Works, Inc.552fccdd-93c4-efff-e063-6294a90a54ba2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Raspberry TangerineALCOHOLBath & Body Works, Inc.552fe6d9-335d-0842-e063-6394a90a98452026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Marine Waves and CitrusALCOHOLBath & Body Works, Inc.552fe62e-5e18-1fed-e063-6294a90a489e2026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Watermelon LemonadeALCOHOLBath & Body Works, Inc.552fe6d9-335f-0842-e063-6394a90a98452026-06-26WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Turquoise WatersALCOHOLBath & Body Works, Inc.552fe62e-5e1e-1fed-e063-6294a90a489e2026-06-26WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.