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DIVALPROEX SODIUM

DIVALPROEX SODIUM · EQ 125MG VALPROIC ACID · TABLET, DELAYED RELEASE · ORAL

ANDA077296HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20080731
Product number
001
Products
  1. Brand name
    DIVALPROEX SODIUM
    Application name
    CHARTWELL RX
    Application type
    A
    Application number
    077296
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    CHARTWELL RX SCIENCES LLC
    Dosage form
    TABLET, DELAYED RELEASE
    Route
    ORAL
    Active ingredients
    1. Name
      DIVALPROEX SODIUM
      Strength
      EQ 125MG VALPROIC ACID
    Therapeutic equivalence codes
    AB
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.