Divalproex Sodium

Product NDC
72162-2460
11-digit product format
721622460
Labeler code
72162
Product ID
72162-2460_92653b4d-75de-4377-9e7e-2b4527826d71
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Divalproex Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA079163
Marketing category
ANDA
Marketing start
2011-10-01
Substance
DIVALPROEX SODIUM
Active strength
250 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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Divalproex Sodium
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIVALPROEX SODIUM250 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii644VL95AO6
Rxcui1099678

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b10a892b-b985-4cbc-9547-9ac4b72b784fProduct name220250818
7a3a03f1-382a-f9ec-0741-ff24dcbfed69Product name720250624
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
57fc3d01-4737-4091-9728-9e8a4c9e708dProduct name120200121
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5d67ecc7-47c7-ec5e-e9eb-71bf00250645Product name120140508
97fce1a8-50c4-f088-0e31-64d82b6e9081Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2460-1Divalproex Sodium100 in 1 BOTTLETABLET, DELAYED RELEASE100102
72162-2460-3Divalproex Sodium30 in 1 BOTTLETABLET, DELAYED RELEASE30102
72162-2460-5Divalproex Sodium500 in 1 BOTTLETABLET, DELAYED RELEASE500102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-2460-1EA - Each72162-24604a7f70a5-81e5-41f0-a64c-60ef0d17b36b12025-05-14
72162-2460-3EA - Each72162-24600d5741dc-641f-44e0-a5a5-81aed729053c12025-05-14
72162-2460-5EA - Each72162-24609a7663f2-632b-4c7f-9178-5897a09a056c12025-05-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2460DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]102Current NDC, 3 package rows20250524_0fb57229-08ef-44d6-b40a-92b2f96ff795.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099678divalproex sodium 250 MG Delayed Release Oral TabletPSN0fb57229-08ef-44d6-b40a-92b2f96ff795102
1099678divalproex sodium 250 MG Delayed Release Oral TabletSCD0fb57229-08ef-44d6-b40a-92b2f96ff795102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-2460-172162246001100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1) 2025-02-21NoNoHistorical
72162-2460-37216224600330 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3) 2025-02-21NoNoHistorical
72162-2460-572162246005500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5) 2025-02-21NoNoHistorical