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PANTOPRAZOLE SODIUM

PANTOPRAZOLE SODIUM · EQ 40MG BASE · TABLET, DELAYED RELEASE · ORAL

ANDA090970HUMAN PRESCRIPTION DRUG
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Approval date
20110119
Product number
002
Products
  1. Brand name
    PANTOPRAZOLE SODIUM
    Application name
    MYLAN PHARMS INC
    Application type
    A
    Application number
    090970
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    MYLAN PHARMACEUTICALS INC
    Dosage form
    TABLET, DELAYED RELEASE
    Route
    ORAL
    Active ingredients
    1. Name
      PANTOPRAZOLE SODIUM
      Strength
      EQ 40MG BASE
    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.