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FESOTERODINE FUMARATE

FESOTERODINE FUMARATE · 8MG · TABLET, EXTENDED RELEASE · ORAL

ANDA204504DISCONTINUED
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Approval date
20230104
Product number
002
Products
  1. Brand name
    FESOTERODINE FUMARATE
    Application name
    ANI PHARMS
    Application type
    A
    Application number
    204504
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    ANI PHARMACEUTICALS INC
    Dosage form
    TABLET, EXTENDED RELEASE
    Route
    ORAL
    Active ingredients
    1. Name
      FESOTERODINE FUMARATE
      Strength
      8MG
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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.