NDC 0832-7124-89 - 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
0832-7124
Requested NDC
0832-7124-89
Package NDCs from labels
0832-7124-11, 0832-7124-15, 0832-7124-89, 0832-7124-01
Manufacturer
Cardinal Health 107, LLC
Effective date
2026-06-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Divalproex Sodium - Cardinal Health 107, LLCCardinal Health 107, LLC2026-06-17HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, IncUpsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc2025-12-11HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - NCS HealthCare of KY, LLC dba Vangard LabsNCS HealthCare of KY, LLC dba Vangard Labs2024-09-17HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - REMEDYREPACK INC.REMEDYREPACK INC.2024-01-09HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - Aphena Pharma Solutions - Tennessee, LLCAphena Pharma Solutions - Tennessee, LLC2018-02-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0832-7124-01Divalproex Sodium100 in 1 CARTONTABLET, DELAYED RELEASE10018
0832-7124-11Divalproex Sodium100 in 1 BOTTLETABLET, DELAYED RELEASE10018
0832-7124-15Divalproex Sodium500 in 1 BOTTLETABLET, DELAYED RELEASE50018
0832-7124-89Divalproex Sodium1 in 1 BLISTER PACKTABLET, DELAYED RELEASE118

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0832-7124DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, LLC]16Current NDC, Legacy NDC, 4 package rows20240726_02304a23-4a5f-47bc-9687-4044b43f7a20.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0832-7124-01EA - Each0832-7124544c0f8e-15ef-4820-aa0b-44c37957f6e512016-04-04
0832-7124-11EA - Each0832-7124fa91b57b-42f4-478b-b9c0-fc2bb21bbf1612014-12-01
0832-7124-15EA - Each0832-71244d2c789b-ff0b-4a88-9224-2b262e01cac912014-07-02
0832-7124-89EA - Each0832-71245c08caf0-6a10-4411-ba34-c517f86b55f212016-04-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Divalproex SodiumACTIVE INGREDIENT644VL95AO6DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
Valproic AcidACTIVE MOIETY614OI1Z5WIDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
FD&C Red No. 40INACTIVE INGREDIENTWZB9127XOADIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
FD&C Yellow No. 6INACTIVE INGREDIENTH77VEI93A8DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
Ferric Oxide RedINACTIVE INGREDIENT1K09F3G675DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type AINACTIVE INGREDIENTNX76LV5T8JDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
povidonesINACTIVE INGREDIENTFZ989GH94EDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
sodium bicarbonateINACTIVE INGREDIENT8MDF5V39QODIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
sodium lauryl sulfateINACTIVE INGREDIENT368GB5141JDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
starch, cornINACTIVE INGREDIENTO8232NY3SJDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
talcINACTIVE INGREDIENT7SEV7J4R1UDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
triethyl citrateINACTIVE INGREDIENT8Z96QXD6UMDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3
vanillinINACTIVE INGREDIENTCHI530446XDIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]3

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 11 of 153 · 3,051 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Divalproex SodiumDIVALPROEX SODIUMA-S Medication Solutions79132bea-04d8-4dd9-bd31-07f0ba805c212026-05-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099625
unii: 644VL95AO6
CalamineCALAMINE AND ZINC OXIDEPharma Nobis, LLCfbcfa541-beda-06de-e053-6294a90a92982026-05-26WarningsExact identifier
unii: 1K09F3G675
Humco Sodium BicarbonateSODIUM BICARBONATEHumco Holding Group, Inc.aeaa34f6-216d-49f3-8393-c7bda96a3e322026-05-26WarningsExact identifier
unii: 8MDF5V39QO
O HUI DAY SHIELD PERFECT SUN BLACK BROAD SPECTRUM SPF 50 SUNSCREENOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDELG H&H Co., Ltd.52ba9423-8b9b-38f7-e063-6394a90a95da2026-05-26WarningsExact identifier
unii: 15FIX9V2JP
RippleGLYCERIN, POVIDONECorneaCare Inc3b5ba197-d501-681e-e063-6294a90aefb52026-05-24WarningsExact identifier
unii: FZ989GH94E
Alka-Seltzer OriginalANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATESelect Consumer Group3ca80d74-1e8b-49d9-e063-6394a90a43122026-05-24WarningsExact identifier
unii: 8MDF5V39QO
Divalproex SodiumDIVALPROEX SODIUMREMEDYREPACK INC.beba3da1-e80d-45b4-9bd6-3ed85c9482f32026-05-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099870
unii: 644VL95AO6
Mineral SPF 30 MoisturizerMINERAL SPF 30 MOISTURIZERDont Run Out Inc (DBA: Public Goods)52462e7e-0c2c-6b64-e063-6394a90a42302026-05-21WarningsExact identifier
unii: 15FIX9V2JP
Divalproex SodiumDIVALPROEX SODIUMBluePoint Laboratoriesb95494e2-ee7a-7415-e053-2995a90ae8522026-05-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099678
rxcui: 1099870
rxcui: 1099625
unii: 644VL95AO6
DRMTLGY Radiance PowderTITANIUM DIOXIDE, ZINC OXIDEDRMTLGY15bda8d5-8c3c-6ba5-e063-6394a90a82d92026-05-21WarningsExact identifier
unii: 15FIX9V2JP
SkinCeuticals Future Mineral UV Defense Invisble Sunscreen Mineral Filters Broad Spectrum SPF 50TITANIUM DIOXIDE AND ZINC OXIDEL'Oreal USA Products Inc0b92a940-0dd4-4266-bd47-88c27def62c02026-05-20WarningsExact identifier
unii: 15FIX9V2JP
WHITENING SUNSCREENANTI WRINKLEWHITENING SUNSCREENANTI WRINKLEShantou Oushiya Biotechnology Co.,Ltd524384e9-b3f8-4c13-e063-6394a90a89732026-05-20WarningsExact identifier
unii: 15FIX9V2JP
IT COSMETICS HELLO SUNSHINE Invisible Sunscreen Broad Spectrum SPF 50 UVA UVB Mineral 50TITANIUM DIOXIDE AND ZINC OXIDEL'Oreal USA Products Inc.fded7dfb-ffb9-4fb0-9511-273e0e1269692026-05-20WarningsExact identifier
unii: 15FIX9V2JP
Freaks of Nature Peak Performance Broad Spectrum SPF 50FREAKS OF NATURE PEAK PERFORMANCE BROAD SPECTRUM SPF 50THE FREAKS OF NATURE, INC.5247187d-a14c-6468-e063-6394a90ace3e2026-05-20WarningsExact identifier
unii: 15FIX9V2JP
Divalproex sodiumDIVALPROEX SODIUMAjanta Pharma USA Inc.773a289b-65ed-4045-80c5-f00e28c1c0792026-05-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Divalproex sodiumDIVALPROEX SODIUMNorthStar Rx LLC589ae3a6-8b2e-d931-d36b-1937287ab5c02026-05-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Divalproex SodiumDIVALPROEX SODIUMRising Pharma Holdings, Inc.6316061c-9758-4f38-9cb2-7ca833dd20bf2026-05-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099678
rxcui: 1099870
rxcui: 1099625
unii: 644VL95AO6
DentaforceANTIMONIUM CRUDUM, BELLADONNA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MERCURIUS SOLUBILIS, PLUMBUM METALLICUM, SEPIA, SILICEA, HYDROFLUORICUM ACIDUMBioActive Nutritional, Inc.82321547-e04a-42ff-aa39-6a192638e5a22026-05-18WarningsExact identifier
unii: ETJ7Z6XBU4
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUMTITANIUM DIOXIDE AND ZINC OXIDELOreal USA Products Inc.23cc5ff4-f842-4e3e-ac5c-23dbaf7d39142026-05-15WarningsExact identifier
unii: 15FIX9V2JP
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUMTITANIUM DIOXIDE AND ZINC OXIDESICOS ET CIEc688f8e6-2cd2-40db-b03f-90fd74c2d89c2026-05-15WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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