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ACYCLOVIR SODIUM

ACYCLOVIR SODIUM · EQ 500MG BASE/VIAL · INJECTABLE · INJECTION

ANDA074663DISCONTINUED
Open FDA's page for this record
Approval date
19970422
Product number
001
Products
  1. Brand name
    ACYCLOVIR SODIUM
    Application name
    HOSPIRA
    Application type
    A
    Application number
    074663
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    HOSPIRA INC
    Dosage form
    INJECTABLE
    Route
    INJECTION
    Active ingredients
    1. Name
      ACYCLOVIR SODIUM
      Strength
      EQ 500MG BASE/VIAL
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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.