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
Label	Manufacturer	Effective date	Type
Divalproex Sodium - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2026-06-17	HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	2025-12-11	HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - NCS HealthCare of KY, LLC dba Vangard Labs	NCS HealthCare of KY, LLC dba Vangard Labs	2024-09-17	HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - REMEDYREPACK INC.	REMEDYREPACK INC.	2024-01-09	HUMAN PRESCRIPTION DRUG LABEL
Divalproex Sodium - Aphena Pharma Solutions - Tennessee, LLC	Aphena Pharma Solutions - Tennessee, LLC	2018-02-16	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0832-7124-01	Divalproex Sodium	100 in 1 CARTON	TABLET, DELAYED RELEASE	100	18
0832-7124-11	Divalproex Sodium	100 in 1 BOTTLE	TABLET, DELAYED RELEASE	100	18
0832-7124-15	Divalproex Sodium	500 in 1 BOTTLE	TABLET, DELAYED RELEASE	500	18
0832-7124-89	Divalproex Sodium	1 in 1 BLISTER PACK	TABLET, DELAYED RELEASE	1	18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0832-7124	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, LLC]	16	Current NDC, Legacy NDC, 4 package rows	20240726_02304a23-4a5f-47bc-9687-4044b43f7a20.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0832-7124-01	EA - Each	0832-7124	544c0f8e-15ef-4820-aa0b-44c37957f6e5	1	2016-04-04
0832-7124-11	EA - Each	0832-7124	fa91b57b-42f4-478b-b9c0-fc2bb21bbf16	1	2014-12-01
0832-7124-15	EA - Each	0832-7124	4d2c789b-ff0b-4a88-9224-2b262e01cac9	1	2014-07-02
0832-7124-89	EA - Each	0832-7124	5c08caf0-6a10-4411-ba34-c517f86b55f2	1	2016-04-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Divalproex Sodium	ACTIVE INGREDIENT	644VL95AO6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
Valproic Acid	ACTIVE MOIETY	614OI1Z5WI	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
FD&C Red No. 40	INACTIVE INGREDIENT	WZB9127XOA	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
FD&C Yellow No. 6	INACTIVE INGREDIENT	H77VEI93A8	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
Ferric Oxide Red	INACTIVE INGREDIENT	1K09F3G675	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type A	INACTIVE INGREDIENT	NX76LV5T8J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
povidones	INACTIVE INGREDIENT	FZ989GH94E	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
sodium bicarbonate	INACTIVE INGREDIENT	8MDF5V39QO	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
talc	INACTIVE INGREDIENT	7SEV7J4R1U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UPSHER-SMITH LABORATORIES, INC.]	3
vanillin	INACTIVE INGREDIENT	CHI530446X	DIVALPROEX 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 109 of 150 · 2,981 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Top Value Effervescent Pain Relief	APIRIN, CITRIC ACID, SODIUM BICARBONATE	Tower Laboratories Ltd	43c7f435-735c-3fab-e054-00144ff88e88	2024-11-13	Warnings, Adverse reactions	Exact identifier unii: 8MDF5V39QO
DG Health Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	DOLGENCORP, INC	8f1343d5-2884-3a14-e053-2a95a90a2f90	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Good Sense Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Good Sense	cd25b0c3-0134-beef-e053-2a95a90a092b	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Drug Mart Effervescent Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Discount Drug Mart, Inc	8bc65603-1dbf-30ab-e053-2995a90a7c15	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Best Choice Effervescent Antacid Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Valu Merchandisers Company	8aab905b-5fe7-dddb-e053-2995a90a6c6f	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Publix Fast Relief Effervescent	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Publix Super Markets Inc.	73051f16-2569-7394-e053-2991aa0a5359	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Quality Choice Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Chain Drug Marketing Association	70d265de-ff94-e0e4-e053-2a91aa0a962a	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Quality Choice Extra Strength Effervescent Antacid and Pain Relief	ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE	Chain Drug Marketing Association	9f7d0c96-a561-a8a0-e053-2995a90a250b	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
WinCo Foods Effervescent Antacid and Pain Relief	ASPIRIN, SODIUM BICARBONATE, CITRIC ACID TABLET	WinCo Foods, LLC	0c8a755a-089f-477f-97e9-0dd6fdfbe99d	2024-11-13	Warnings	Exact identifier unii: 8MDF5V39QO
Focus	ADENOSINUM CYCLOPHOSPHORICUM, ADRENALINUM, AETHUSA CYNAPIUM, ALPHA-KETOGLUTARICUM ACIDUM, AMBRA GRISEA, BARYTA CARBONICA, CANDIDA ALBICANS, CARBONEUM SULPHURATUM, CEREBRUM SUIS, GINKGO BILOBA, HELLEBORUS NIGER, HYPOTHALAMUS SUIS, HYOSCYAMUS NIGER, IODIUM, PHOSPHORUS, SACCHARUM OFFICINALE, SARCOLACTICUM ACID, SILICEA, TARENTULA HISPANA, VERATRUM ALBUM	Deseret Biologicals, Inc.	e014e6b6-a07a-4170-b9af-f477da71597d	2024-11-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Kenvue Brands LLC	18e40353-5c95-4d64-e063-6394a90a017c	2024-11-12	Warnings	Exact identifier unii: 15FIX9V2JP
Neutrogena Healthy Skin Liquid Makeup SPF 20 - Classic Ivory 10	TITANIUM DIOXIDE	Kenvue Brands LLC	e0ed4537-8146-45e8-e053-2995a90ac51b	2024-11-12	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 4.5W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	504d8118-f84d-4f3f-abd1-463f3780a2cb	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 2WO	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	0d4e667a-cf93-4f6d-8565-ecfa9a18cfbf	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 2.5W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	cb1d643e-34dc-48f2-aecd-ba2a35dc3403	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 2W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	097b3d7b-5dff-4206-99f1-6573902232e9	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 4W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	a621a610-7dd2-4ccd-bc48-8671e4f4a887	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 3W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	43296d42-7bc2-4073-8231-4a7921f9ebe3	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 6N	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	5ee35643-bd86-4d55-914a-96f4670bfd07	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 4WP	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	f519aa3f-11a1-4941-bf31-47ac11f5a703	2024-11-11	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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