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HALOPERIDOL

HALOPERIDOL · 10MG · TABLET · ORAL

ANDA077580HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20071129
Product number
004
Products
  1. Brand name
    HALOPERIDOL
    Application name
    ZYDUS PHARMS USA
    Application type
    A
    Application number
    077580
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    ZYDUS PHARMACEUTICALS USA INC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      HALOPERIDOL
      Strength
      10MG
    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.