NDC 64679-973

DIVALPROEX SODIUM

Divalproex Sodium

DIVALPROEX SODIUM is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Divalproex Sodium.

Product ID64679-973_a52fc616-0332-4ba1-bb2f-50e5ac8da6f9
NDC64679-973
Product TypeHuman Prescription Drug
Proprietary NameDIVALPROEX SODIUM
Generic NameDivalproex Sodium
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2008-07-31
Marketing CategoryANDA / ANDA
Application NumberANDA077296
Labeler NameWockhardt USA LLC.
Substance NameDIVALPROEX SODIUM
Active Ingredient Strength125 mg/1
Pharm ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 64679-973-03

30 TABLET, DELAYED RELEASE in 1 BOTTLE (64679-973-03)
Marketing Start Date2008-07-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-973-04 [64679097304]

DIVALPROEX SODIUM TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077296
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-07-31
Inactivation Date2020-01-31

NDC 64679-973-02 [64679097302]

DIVALPROEX SODIUM TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077296
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-07-31
Inactivation Date2020-01-31

NDC 64679-973-03 [64679097303]

DIVALPROEX SODIUM TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077296
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-07-31
Inactivation Date2020-01-31

NDC 64679-973-01 [64679097301]

DIVALPROEX SODIUM TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA077296
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-07-31
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DIVALPROEX SODIUM125 mg/1

OpenFDA Data

SPL SET ID:cd83f986-ec38-4e0e-aa03-3db5ad1629c6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1099870
  • 1099625
  • 1099678
    • UPC Code
  • 0364679975022
  • 0364679974018

    • Pharmacological Class

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

    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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