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DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE

DORZOLAMIDE HYDROCHLORIDE, TIMOLOL MALEATE · EQ 2% BASE, EQ 0.5% BASE · SOLUTION/DROPS · OPHTHALMIC

ANDA090604HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20091118
Product number
001
Products
  1. Brand name
    DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE
    Application name
    SANDOZ
    Application type
    A
    Application number
    090604
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    SANDOZ INC
    Dosage form
    SOLUTION/DROPS
    Route
    OPHTHALMIC
    Active ingredients
    1. Name
      DORZOLAMIDE HYDROCHLORIDE
      Strength
      EQ 2% BASE
    2. Name
      TIMOLOL MALEATE
      Strength
      EQ 0.5% BASE
    Therapeutic equivalence codes
    AT1
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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.