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 85 of 325 · 6,482 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Isopropyl alcohol 50 percentISOPROPYL ALCOHOLEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)b1b52183-3296-48b2-b3d3-821c141b0bea2026-02-05WarningsExact identifier
unii: ND2M416302
Isopropyl alcohol 50 percentISOPROPYL ALCOHOLEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)ee67fb96-fa2c-4542-8fdb-f2ccd885ee532026-02-05WarningsExact identifier
unii: ND2M416302
DPT-TOXDROSERA, ECHINACEA, HYPERICUM, KALI MUR, MEZEREUM, SILICEA, THUJANutrition Center Inc dba Nutri-West dba Micro-West5e39f4e6-939f-4b71-9cc5-6d4b8711ea322026-02-04WarningsExact identifier
unii: ETJ7Z6XBU4
SHISEIDO URBAN ENVIRONMENT oil-free MINERAL SUNSCREEN SPF 42TITANIUM DIOXIDE AND ZINC OXIDESHISEIDO AMERICAS CORPORATION86630e82-f249-4866-82dd-3e21feb266c42026-02-04WarningsExact identifier
unii: 15FIX9V2JP
Isopropyl AlcoholISOPROPYL ALCOHOLDyad Medical Sourcing, LLCb5c9e222-10eb-4cea-af70-213a77fcc8652026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Tork Hand Sanitizing Alcohol FoamALCOHOLEssity Professional Hygiene North America LLC3987934e-2bf9-4c80-8842-2ad294e485862026-02-04WarningsExact identifier
unii: 3K9958V90M
Ethyl AlcoholETHYL ALCOHOLGeorgia-Pacific Consumer Products LPa935425d-f86b-41e9-bbce-1a028e302e102026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
enMotion Foam High Frequency UseETHYL ALCOHOLGeorgia-Pacific Consumer Products LPe56f5a94-0be1-487b-ad95-c1fe74c824ee2026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Pacific Blue Ultra Foaming Fragrance FreeETHYL ALCOHOLGeorgia-Pacific Consumer Products LP0bdc1b9a-0a56-466b-ac51-95c499e909782026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
enMotion Foam with Moisturizers fragrance freeETHYL ALCOHOLGeorgia-Pacific Consumer Products LP6f0b8537-fe1f-4265-ab1a-e869d16fb60e2026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Isopropyl AlcoholISOPROPYL ALCOHOLGoBrands, Inc.0fb3db50-4132-07dc-e063-6294a90a81682026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLGrocery Outlet, Inc.3dff8c83-7c33-7bca-e063-6394a90a675f2026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl alcoholISOPROPYL ALCOHOLGrocery Outlet, Inc.3dffba95-71c4-a2b0-e063-6394a90aaeb32026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Hand SanitizerALCOHOLHarris Teeter0bb08a9f-55af-4ccb-a848-3f58c55645a92026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Advanced Hand SanitizerETHYL ALCOHOLHarris Teeterbb08034b-9516-435a-bbc3-888e9dbaccbf2026-02-04Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Japanese Cherry BlossomALCOHOLBath & Body Works, Inc.1ac8bbdb-087a-d966-e063-6394a90aa4332026-02-04WarningsExact identifier
unii: 3K9958V90M
91% ISOPROPYL ALCOHOL91% ISOPROPYL ALCOHOLHy-Vee, Inc.497471bb-541c-f945-e063-6294a90adbb22026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl Rubbing AlcoholISOPROPYL RUBBING ALCOHOLHy-Vee, Inc.4831eecf-d111-6f17-e063-6394a90a4ab92026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302
CalamineFERRIC OXIDE REDMajor Pharmaceuticalsc25be68d-834a-4959-8d47-01ec789406ba2026-02-04Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
Anti Bacterial Hand Gel Into The NightALCOHOLBath & Body Works, Inc.1ac714c0-d55b-e308-e063-6394a90ac64b2026-02-04WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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