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DILTIAZEM HYDROCHLORIDE

DILTIAZEM HYDROCHLORIDE · 30MG · TABLET · ORAL

ANDA074084DISCONTINUED
Open FDA's page for this record
Approval date
19940225
Product number
001
Products
  1. Brand name
    DILTIAZEM HYDROCHLORIDE
    Application name
    TEVA
    Application type
    A
    Application number
    074084
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    TEVA PHARMACEUTICALS USA INC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      DILTIAZEM HYDROCHLORIDE
      Strength
      30MG
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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.