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PRAMIPEXOLE DIHYDROCHLORIDE

PRAMIPEXOLE DIHYDROCHLORIDE · 0.5MG · TABLET · ORAL

ANDA090241DISCONTINUED
Open FDA's page for this record
Approval date
20101008
Product number
003
Products
  1. Brand name
    PRAMIPEXOLE DIHYDROCHLORIDE
    Application name
    CHARTWELL RX
    Application type
    A
    Application number
    090241
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    CHARTWELL RX SCIENCES LLC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      PRAMIPEXOLE DIHYDROCHLORIDE
      Strength
      0.5MG
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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.