Home NDC 65862-784-10 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 Package Descriptions# Package NDC, Product, Description table 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# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65862-784 ESOMEPRAZOLE MAGNESIUM CAPSULE, DELAYED RELEASE [AUROBINDO PHARMA LIMITED] 15 Current NDC, Legacy NDC, 6 package rows 20250417_f4ae091d-9b74-4a0e-ac68-057effd91e17.zip
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 227 of 323 · 6,449 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join germstarGel ETHYL ALCOHOL Soaptronic, LLC b5fd6c3c-d452-74e6-e053-2995a90a9090 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cucumber Melon ALCOHOL Bath & Body Works, Inc. 29a63c54-116f-30bb-e063-6394a90a8c6f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Frosted Coconut Snowball ALCOHOL Bath & Body Works, Inc. 29a652a8-15fd-80d4-e063-6394a90acb4d 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Black Cherry Frost ALCOHOL Bath & Body Works, Inc. 29a654df-016b-830e-e063-6394a90a1062 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Winterberry Ice ALCOHOL Bath & Body Works, Inc. 29a64c95-eb54-8081-e063-6394a90a0726 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Magic In The Air ALCOHOL Bath & Body Works, Inc. 29a651e4-a014-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Tea and Lemonade ALCOHOL Bath & Body Works, Inc. 29a64de5-af39-5a91-e063-6394a90ac35c 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Honolulu Sun ALCOHOL Bath & Body Works, Inc. 29a64c62-8517-1b39-e063-6294a90a35a8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Snowflakes ALCOHOL Bath & Body Works, Inc. 29a651e4-a016-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Snowflakes and Cashmere ALCOHOL Bath & Body Works, Inc. 29a654df-0169-830e-e063-6394a90a1062 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CARAMEL OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE COSMAX USA, INC 29a82ba9-c0f8-0edf-e063-6294a90a50b4 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SABLE OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE COSMAX USA, INC 29a8812b-70ff-e8aa-e063-6294a90a09f8 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Neutral Deep TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE KW ABSC, INC. 3a548deb-3670-4c5b-a139-796701801fed 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Olive Medium Deep TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. be4434c0-cbdd-46cb-8015-4c7859e80d4a 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Golden Medium TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. de50e956-a014-4147-922b-63c95fa6f86b 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Neutral Light TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. 44cbb226-83ed-401b-baf8-ca8e4740dbef 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Neutral Medium Light TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. 615f5e39-695d-41d4-af59-e0d3b76789bb 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Warm Deep TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE KW ABSC, INC. 6ab3e360-8104-4439-93fb-e11bc4a77558 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Neutral Medium TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. a297ff64-678c-4936-8384-022606a2f33c 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP CLE CCC Neutral Fair TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE KW ABSC, INC. aa8176c6-f1c9-43dd-96e0-f7d6ed30a1a2 2024-12-19 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.