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 79 of 325 · 6,482 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Isopropyl AlcoholISOPROPYL ALCOHOLTarget Corporationb5455e53-2b86-48e7-a479-664f6601bab72026-02-18Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Travel Wipes Fresh Citrus ScentALCOHOLSINGULAR ENTERPRISES LLCea77be5e-7c69-4787-b39a-4753b002dbbd2026-02-18WarningsExact identifier
unii: 3K9958V90M
Travel Wipes UnscentedISOPROPYL ALCOHOLSINGULAR ENTERPRISES LLCdd046146-fda7-438c-98ca-96ea1dd0ae0b2026-02-18WarningsExact identifier
unii: ND2M416302
70%ISOPROPYL ALCOHOLTarget Corporation4db7c9cb-021d-463a-9ff6-91ae42f0311d2026-02-18Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Antibacterial Hand SanitizerALCOHOLS. P. Richards Company8d88285b-83d5-4089-bb8d-839537ae06f52026-02-18Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Mitochondria ProARALIA QUINQUEFOLIA, ARNICA MONTANA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, ASCORBICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, CALCAREA CARBONICA, CITRICUM ACIDUM, CUPRUM METALLICUM, CYSTEINUM, FERRUM METALLICUM, IODIUM, LEVOTHYROXINUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM ACETICUM, NADIDUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SELENIUM METALLICUM, SULPHUR, THIAMINUM HYDROCHLORICUM, UBIDECARENONUM, ZINCUM METALLICUM,Energique, Inc.2f365207-b730-428d-9465-8853e86e79ff2026-02-18WarningsExact identifier
unii: ETJ7Z6XBU4
BCBG GENERATION HAND SANITIZER MALIBU Peach SCENTETHYL ALCOHOLDiamond Life Cosmetics Trading FZCO8579e94a-b83d-4720-838e-a36368642deb2026-02-18WarningsExact identifier
unii: 3K9958V90M
BCBG GENERATION HAND SANITIZER PINK Guava SCENTETHYL ALCOHOLDIAMOND LIFE COSMETICS TRADING FZCOe950cb8f-b6dc-4cde-8027-e5ca1c0e4e222026-02-18WarningsExact identifier
unii: 3K9958V90M
SOUR LEMON Hand Sanitizer JUNIPER BERRY SCENTETHYL ALCOHOLDiamond Life Cosmetics Trading FZCOf5693209-7adf-43fd-87b1-1c8819c2db6c2026-02-17WarningsExact identifier
unii: 3K9958V90M
Smart Care VANILLA HEAVEN HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.19163896-3ac4-413d-8072-53776712f3cd2026-02-17WarningsExact identifier
unii: 3K9958V90M
Smart Care ISLAND MANGO HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.71e3d290-452d-4854-9ce5-47041f7472502026-02-17WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer with AloeALCOHOLUpLift Brands, LLC3b4d4901-cf7d-4048-8a24-cfb00fd8b1082026-02-17Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
BIO COM 25 ACIDITYNAT PHOS, NAT SULPH, SILICEABM Private Limited3b3c3455-b321-071d-e063-6394a90a01602026-02-17WarningsExact identifier
unii: ETJ7Z6XBU4
Wintergreen 91 - Iron LabETHYL ALCOHOLIron Lab SA de CV323a0717-0d61-c911-e063-6394a90a48542026-02-17WarningsExact identifier
unii: 3K9958V90M
Ethyl Rubbing AlcoholALCOHOLIron Lab SA de CV323b2f5d-34b9-8f5b-e063-6394a90a59d52026-02-17WarningsExact identifier
unii: 3K9958V90M
50 Ethyl Rubbing AlcoholALCOHOLIron Lab SA de CV323b7ff8-91ce-c7a4-e063-6394a90a69fc2026-02-17WarningsExact identifier
unii: 3K9958V90M
70 Alcohol Hand SanitizerALCOHOLIron Lab SA de CV323c06d5-c984-39b8-e063-6294a90a0d3f2026-02-17WarningsExact identifier
unii: 3K9958V90M
50 Wintergreen AlcoholALCOHOLIron Lab SA de CV323baeb1-e3ee-ec70-e063-6294a90a30f02026-02-17WarningsExact identifier
unii: 3K9958V90M
70 Rubbing Ethyl AlcoholALCOHOLIron Lab SA de CV323be8b4-4588-e2a6-e063-6394a90ab68b2026-02-17WarningsExact identifier
unii: 3K9958V90M
AlcoholALCOHOLUnited Natural Foods, Inc. dba UNFIb63d9c12-8471-4db5-998b-ab46184495372026-02-17Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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