NDC 65862-402

Divalproex Sodium

Divalproex Sodium

Divalproex Sodium is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Divalproex Sodium.

Product ID65862-402_301765e8-7397-4a96-b204-a6b75ee6876d
NDC65862-402
Product TypeHuman Prescription Drug
Proprietary NameDivalproex Sodium
Generic NameDivalproex Sodium
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2014-10-24
Marketing CategoryANDA / ANDA
Application NumberANDA090554
Labeler NameAurobindo Pharma Limited
Substance NameDIVALPROEX SODIUM
Active Ingredient Strength250 mg/1
Pharm ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 65862-402-01

100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-01)
Marketing Start Date2014-10-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-402-99 [65862040299]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA090554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-24

NDC 65862-402-10 [65862040210]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA090554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-24

NDC 65862-402-01 [65862040201]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA090554
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-24

NDC 65862-402-05 [65862040205]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA090554
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-24

NDC 65862-402-39 [65862040239]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA090554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-10-24

Drug Details

Active Ingredients

IngredientStrength
DIVALPROEX SODIUM250 mg/1

OpenFDA Data

SPL SET ID:dbd47222-14f1-4588-a009-9b81b55ca60d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1099870
  • 1099625
  • 1099678
  • Pharmacological Class

    • Anti-epileptic Agent [EPC]
    • Decreased Central Nervous System Disorganized Electrical Activity [PE]
    • Mood Stabilizer [EPC]

    Medicade Reported Pricing

    65862040205 DIVALPROEX SOD DR 250 MG TAB

    Pricing Unit: EA | Drug Type:

    65862040201 DIVALPROEX SOD DR 250 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Divalproex Sodium" or generic name "Divalproex Sodium"

    NDCBrand NameGeneric Name
    68001-105Divalproex SodiumDivalproex Sodium
    68001-106Divalproex SodiumDivalproex Sodium
    68071-4102Divalproex SodiumDivalproex Sodium
    68084-313divalproex sodiumdivalproex sodium
    68084-310Divalproex SodiumDivalproex Sodium
    68084-415Divalproex SodiumDivalproex Sodium
    68084-782Divalproex SodiumDivalproex Sodium
    68084-776Divalproex SodiumDivalproex Sodium
    68151-1164Divalproex SodiumDivalproex Sodium
    68151-4162Divalproex SodiumDivalproex Sodium
    68180-266Divalproex SodiumDivalproex Sodium
    68180-267Divalproex SodiumDivalproex Sodium
    68180-265Divalproex SodiumDivalproex Sodium
    68382-032Divalproex SodiumDivalproex Sodium
    68382-033Divalproex SodiumDivalproex Sodium
    68382-031Divalproex SodiumDivalproex Sodium
    68382-133Divalproex SodiumDivalproex Sodium
    68382-134Divalproex SodiumDivalproex Sodium
    68382-106divalproex sodiumdivalproex sodium
    68788-7183Divalproex SodiumDivalproex Sodium
    68788-7295Divalproex SodiumDivalproex Sodium
    68788-7177Divalproex sodiumDivalproex sodium
    69189-0046Divalproex SodiumDivalproex Sodium
    70518-0282Divalproex SodiumDivalproex Sodium
    70518-0312Divalproex SodiumDivalproex Sodium
    70518-0463Divalproex SodiumDivalproex Sodium
    70518-0613Divalproex SodiumDivalproex Sodium
    70518-0374Divalproex SodiumDivalproex Sodium
    70518-1556Divalproex SodiumDivalproex Sodium
    70518-1661Divalproex SodiumDivalproex Sodium
    70518-1138Divalproex SodiumDivalproex Sodium
    70518-1781Divalproex sodiumDivalproex sodium
    70518-1749divalproex sodiumdivalproex sodium
    70518-1558Divalproex SodiumDivalproex Sodium
    70518-1897Divalproex sodiumDivalproex sodium
    0615-1393Divalproex sodiumDivalproex sodium
    71335-0008Divalproex SodiumDivalproex Sodium
    71610-205Divalproex sodiumDivalproex sodium
    71610-032Divalproex SodiumDivalproex Sodium
    71610-157Divalproex sodiumDivalproex sodium
    71610-201Divalproex SodiumDivalproex Sodium
    71610-030Divalproex SodiumDivalproex Sodium
    0615-7532Divalproex SodiumDivalproex Sodium
    0615-7531Divalproex SodiumDivalproex Sodium
    0615-7533Divalproex SodiumDivalproex Sodium
    0615-7554Divalproex SodiumDivalproex Sodium
    71610-031Divalproex SodiumDivalproex Sodium
    0615-7555Divalproex SodiumDivalproex Sodium
    0615-7848Divalproex SodiumDivalproex Sodium
    0615-7950Divalproex SodiumDivalproex Sodium

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