FDA.reportPublic FDA data

NDC 50090-2007-01 - Divalproex Sodium

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
50090-2007
Requested NDC
50090-2007-01
Package NDCs from labels
50090-2007-0, 50090-2007-1, 50090-2007-01
Manufacturer
A-S Medication Solutions
Effective date
2024-04-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Divalproex Sodium - A-S Medication SolutionsA-S Medication Solutions2024-04-23HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
50090-2007-02023-02-07These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-12023-02-07These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-02023-01-30These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-12023-01-30These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2007-0Divalproex Sodium30 in 1 BOTTLETABLET, DELAYED RELEASE3022
50090-2007-1Divalproex Sodium100 in 1 BOTTLETABLET, DELAYED RELEASE10022

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2007DIVALPROEX SODIUM TABLET, DELAYED RELEASE [A-S MEDICATION SOLUTIONS]22Current NDC, Legacy NDC, 2 package rows20240425_8ecfe765-d743-4308-9cd9-4a7b1a229ea9.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2007-0EA - Each50090-200755da1874-9b47-405d-b48c-79c1eb4dfd3b12018-12-13
50090-2007-1EA - Each50090-2007aaa8d9ba-d520-4e69-ab5d-43c9b77ed4e312021-09-07

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 49 of 328 · 6,556 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
divalproex sodiumDIVALPROEX SODIUMREMEDYREPACK INC.ab8616a5-ea72-4df7-b095-54ea19ef6fba2026-04-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Divalproex SodiumDIVALPROEX SODIUMREMEDYREPACK INC.ed24bb3a-bba1-4b27-8733-96619793fc152026-04-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099870
unii: 644VL95AO6
Tru Skin Rituals SPF 25TITANIUM DIOXIDE, ZINC OXIDESpa de Soleilf725cd5c-999e-2393-e053-6394a90a09dc2026-04-30WarningsExact identifier
unii: 15FIX9V2JP
divalproex sodiumDIVALPROEX SODIUMBionpharma Inc.19064624-81d1-4ce3-bfe4-955bad6af6a22026-04-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099678
rxcui: 1099870
rxcui: 1099625
unii: 644VL95AO6
meijer APPLE SCENTED Hand SanitizerETHYL ALCOHOLMeijer, Inc.502e471d-fe0a-1d82-e063-6294a90a376d2026-04-30WarningsExact identifier
unii: 3K9958V90M
Hydrate ICOFFEA TOSTA, GINKGO BILOBA, GERMANIUM SESQUIOXIDE, SILICEABioActive Nutritional, Inc.c0c8d350-0257-4484-acd8-f852350173db2026-04-30WarningsExact identifier
unii: ETJ7Z6XBU4
Ethyl Rubbing AlcoholETHYL ALCOHOLYour Military Exchanges3dce175c-f893-4cfc-b495-6c11f2b77b872026-04-29Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Isopropyl AlcoholISOPROPYL ALCOHOLPerrigo Direct, Inc11d89d11-103e-4ef6-a996-65cff67f9b322026-04-29Warnings, Adverse reactionsExact identifier
unii: ND2M416302
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals Ltd.509cad98-0321-2a0a-e063-6294a90a6ea92026-04-29WarningsExact identifier
unii: 15FIX9V2JP
Isopropyl AlcoholISOPROPYL ALCOHOLWalmart Inc.1fd3d29f-7da0-c5ba-e063-6294a90add162026-04-29Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Summit 375 Gel Alcohol Hand SanitizerALCOHOLR.L. Williams Company509cc442-09f8-d17f-e063-6394a90a77ea2026-04-29WarningsExact identifier
unii: 3K9958V90M
Ethyl AlcoholETHYL ALCOHOLWalmart Inc.1fd3bed0-8fcc-2cee-e063-6294a90a34fb2026-04-29Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals Ltd.509d7206-0cc1-c997-e063-6294a90a89e02026-04-29WarningsExact identifier
unii: 15FIX9V2JP
iVIZIA Lubricant Eye GelPOVIDONEThea Pharma Inc.1f06ca1a-5270-9a82-e063-6294a90aed642026-04-29WarningsExact identifier
unii: FZ989GH94E
MHB SKIN HYDRATING HAND SANITIZER, LILY MISTALCOHOL HAND SANITIZERCROWN (YANGZHOU) HEALTH & BEAUTY CO., LTD.50949ae2-3ebe-08d2-e063-6394a90a20462026-04-29WarningsExact identifier
unii: 3K9958V90M
MHB SKIN HYDRATING HAND SANITIZER SANTAL WAVE 35mlALCOHOL HAND SANITIZERCROWN (YANGZHOU) HEALTH & BEAUTY CO., LTD.493120ee-0c5c-b704-e063-6394a90a8c192026-04-29WarningsExact identifier
unii: 3K9958V90M
JMSOLUTION SKIN BOOST NIACINAMIDE SUNSCREENHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEGPNY CORP211dea04-faad-8ffc-e063-6294a90a8d682026-04-29WarningsExact identifier
unii: 15FIX9V2JP
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLPreferred PHarmaceuticals Inc.011473a8-26d5-4661-b3c0-745f9b6aa1d82026-04-29WarningsExact identifier
unii: FZ989GH94E
divalproex sodiumDIVALPROEX SODIUMFirst Nation Group, LLCa76f9909-28c9-4eb7-8ffd-ff6222fea0792026-04-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
B-Pure Moisturizing Hand Sanitizer Vanilla Creme ScentedALCOHOLFourstar Group USA, Inc.13faded0-7953-4d86-b952-e4bcf4ba53cc2026-04-28WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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