Depakote

Product NDC
0074-6114
11-digit product format
000746114
Labeler code
0074
Product ID
0074-6114_d038b7e9-b014-4771-93be-90aeeaece03d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Divalproex Sodium
Dosage form
CAPSULE
Route
ORAL
Labeler
AbbVie Inc.
Application
NDA019680
Marketing category
NDA
Marketing start
1989-09-12
Substance
DIVALPROEX SODIUM
Active strength
125 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Depakote
Brand name suffix
Sprinkles
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIVALPROEX SODIUM125 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii644VL95AO6
Rxcui1099596, 1099598

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b10a892b-b985-4cbc-9547-9ac4b72b784fProduct name220250818
7a3a03f1-382a-f9ec-0741-ff24dcbfed69Product name720250624
57fc3d01-4737-4091-9728-9e8a4c9e708dProduct name120200121
5d67ecc7-47c7-ec5e-e9eb-71bf00250645Product name120140508
97fce1a8-50c4-f088-0e31-64d82b6e9081Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0074-6114-11DepakoteSprinkles10 in 1 BLISTER PACKCAPSULE101631
0074-6114-11DepakoteSprinkles10 in 1 CARTONCAPSULE101631
0074-6114-13DepakoteSprinkles100 in 1 BOTTLECAPSULE1001631

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0074-6114-11EA - Each0074-6114ab7a3dc0-6a48-496b-b425-8e5130cf9b6d12012-07-24
0074-6114-13EA - Each0074-611412fd956a-f652-433f-ab1d-320e7563774012012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0074-6114DEPAKOTE SPRINKLES (DIVALPROEX SODIUM) CAPSULE [ABBVIE INC.]1628Current NDC, Legacy NDC, 3 package rows20250519_4619aff4-0f80-444f-858d-42e4137aa809.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099598Depakote 125 MG Delayed Release Oral Sprinkle CapsulePSN4619aff4-0f80-444f-858d-42e4137aa8091631
1099596divalproex sodium 125 MG Delayed Release Oral CapsulePSN4619aff4-0f80-444f-858d-42e4137aa8091631
1099598divalproex sodium 125 MG Delayed Release Oral Capsule [Depakote]SBD4619aff4-0f80-444f-858d-42e4137aa8091631
1099596divalproex sodium 125 MG Delayed Release Oral CapsuleSCD4619aff4-0f80-444f-858d-42e4137aa8091631
1099598Depakote 125 MG Delayed Release Oral CapsuleSY4619aff4-0f80-444f-858d-42e4137aa8091631
1099598Depakote Sprinkle 125 MG Delayed Release Oral CapsuleSY4619aff4-0f80-444f-858d-42e4137aa8091631

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0074-6114-110007461141110 in 1 BLISTER PACKHistorical
0074-6114-1300074611413100 CAPSULE in 1 BOTTLE (0074-6114-13) 100 capsule1989-09-120000-00-00NoNoCurrent