NDC 64679-974

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 ID64679-974_a52fc616-0332-4ba1-bb2f-50e5ac8da6f9
NDC64679-974
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 Strength250 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 64679-974-02

500 TABLET, DELAYED RELEASE in 1 BOTTLE (64679-974-02)
Marketing Start Date2008-07-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-974-03 [64679097403]

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

NDC 64679-974-04 [64679097404]

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

NDC 64679-974-02 [64679097402]

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

NDC 64679-974-01 [64679097401]

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 SODIUM250 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.