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PREDNISOLONE

PREDNISOLONE · 5MG · TABLET · ORAL

ANDA085085DISCONTINUED
Open FDA's page for this record
Approved prior to 1982
true
Product number
002
Products
  1. Brand name
    PREDNISOLONE
    Application name
    WATSON LABS
    Application type
    A
    Application number
    085085
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    WATSON LABORATORIES INC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      PREDNISOLONE
      Strength
      5MG
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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.