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CYCLOSPORINE

CYCLOSPORINE · 100MG/ML · SOLUTION · ORAL

ANDA065078HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20050325
Product number
001
Products
  1. Brand name
    CYCLOSPORINE
    Application name
    IVAX SUB TEVA PHARMS
    Application type
    A
    Application number
    065078
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
    Dosage form
    SOLUTION
    Route
    ORAL
    Active ingredients
    1. Name
      CYCLOSPORINE
      Strength
      100MG/ML
    Therapeutic equivalence codes
    AB1
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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.