NDC 64679-725

Divalproex Sodium ER

Divalproex Sodium

Divalproex Sodium ER is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Divalproex Sodium.

Product ID64679-725_0d656d32-d508-4fda-8ffd-2f14c584fd7c
NDC64679-725
Product TypeHuman Prescription Drug
Proprietary NameDivalproex Sodium ER
Generic NameDivalproex Sodium
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2009-08-04
Marketing CategoryANDA / ANDA
Application NumberANDA078705
Labeler NameWockhardt USA LLC.
Substance NameDIVALPROEX SODIUM
Active Ingredient Strength500 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 64679-725-01

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-725-01)
Marketing Start Date2009-08-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-725-04 [64679072504]

Divalproex Sodium ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078705
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-08-04

NDC 64679-725-03 [64679072503]

Divalproex Sodium ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078705
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-08-04

NDC 64679-725-01 [64679072501]

Divalproex Sodium ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078705
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-08-04

NDC 64679-725-02 [64679072502]

Divalproex Sodium ER TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078705
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-08-04

Drug Details

Active Ingredients

IngredientStrength
DIVALPROEX SODIUM500 mg/1

OpenFDA Data

SPL SET ID:a93b0914-c1ac-4e48-b6b9-1b4e211eb072
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1099563
  • 1099569
    • UPC Code
  • 0364679725023
  • 0364679724026

    • Pharmacological Class

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

    Medicade Reported Pricing

    64679072503 DIVALPROEX SOD ER 500 MG TAB

    Pricing Unit: EA | Drug Type:

    64679072502 DIVALPROEX SOD ER 500 MG TAB

    Pricing Unit: EA | Drug Type:

    64679072501 DIVALPROEX SOD ER 500 MG TAB

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    55648-724DIVALPROEX SODIUM ERDIVALPROEX SODIUM ER
    55648-725DIVALPROEX SODIUM ERDIVALPROEX SODIUM ER
    64679-725Divalproex Sodium ERDivalproex Sodium ER
    64679-724Divalproex Sodium ERDivalproex Sodium ER
    0074-3826DepakoteDivalproex Sodium
    0074-6114DepakoteDivalproex Sodium
    0074-6212DepakoteDivalproex Sodium
    0074-6214DepakoteDivalproex Sodium
    0074-6215DepakoteDivalproex Sodium
    0074-7126DepakoteDivalproex Sodium
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