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OXYCODONE HYDROCHLORIDE

OXYCODONE HYDROCHLORIDE · 5MG · TABLET · ORAL

ANDA076636DISCONTINUED
Open FDA's page for this record
Approval date
20150407
Product number
003
Products
  1. Brand name
    OXYCODONE HYDROCHLORIDE
    Application name
    ACTAVIS ELIZABETH
    Application type
    A
    Application number
    076636
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    ACTAVIS ELIZABETH LLC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      OXYCODONE HYDROCHLORIDE
      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.