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ESTRADIOL

ESTRADIOL · 0.5MG · TABLET · ORAL

ANDA040138DISCONTINUED
Open FDA's page for this record
Approval date
19980130
Product number
001
Products
  1. Brand name
    ESTRADIOL
    Application name
    LANNETT CO INC
    Application type
    A
    Application number
    040138
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    LANNETT CO INC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      ESTRADIOL
      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.