Approvals (Drugs@FDA)

LOSARTAN POTASSIUM

APOTEX · LOSARTAN POTASSIUM

ANDA218551Generic (ANDA)Discontinued
Open FDA's page for this record
Application number
ANDA218551
Sponsor name
APOTEX
Submissions
  1. Submission type
    SUPPL
    Submission number
    1
    Submission status
    AP
    Submission status date
    20250909
    Review priority
    STANDARD
    Submission class code
    LABELING
    Submission class code description
    Labeling
  2. Submission type
    ORIG
    Submission number
    1
    Submission status
    AP
    Submission status date
    20240604
    Review priority
    STANDARD
    Submission class code
    UNKNOWN
Products
  1. Product number
    003
    Reference drug
    No
    Brand name
    LOSARTAN POTASSIUM
    Reference standard
    No
    Dosage form
    TABLET
    Route
    ORAL
    Marketing status
    Discontinued
    Te code
    AB
    Active ingredients
    1. Name
      LOSARTAN POTASSIUM
      Strength
      100MG
  2. Product number
    001
    Reference drug
    No
    Brand name
    LOSARTAN POTASSIUM
    Reference standard
    No
    Dosage form
    TABLET
    Route
    ORAL
    Marketing status
    Discontinued
    Te code
    AB
    Active ingredients
    1. Name
      LOSARTAN POTASSIUM
      Strength
      25MG
  3. Product number
    002
    Reference drug
    No
    Brand name
    LOSARTAN POTASSIUM
    Reference standard
    No
    Dosage form
    TABLET
    Route
    ORAL
    Marketing status
    Discontinued
    Te code
    AB
    Active ingredients
    1. Name
      LOSARTAN POTASSIUM
      Strength
      50MG
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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.