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BENDAMUSTINE HYDROCHLORIDE

BENDAMUSTINE HYDROCHLORIDE · 25MG/VIAL · POWDER · INTRAVENOUS

ANDA205574HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20221207
Product number
001
Products
  1. Brand name
    BENDAMUSTINE HYDROCHLORIDE
    Application name
    ACCORD HLTHCARE
    Application type
    A
    Application number
    205574
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    ACCORD HEALTHCARE INC
    Dosage form
    POWDER
    Route
    INTRAVENOUS
    Active ingredients
    1. Name
      BENDAMUSTINE HYDROCHLORIDE
      Strength
      25MG/VIAL
    Therapeutic equivalence codes
    AP
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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.