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PROCHLORPERAZINE EDISYLATE

PROCHLORPERAZINE EDISYLATE · EQ 5MG BASE/5ML · SYRUP · ORAL

ANDA087154DISCONTINUED
Open FDA's page for this record
Approval date
19820901
Product number
001
Products
  1. Brand name
    PROCHLORPERAZINE EDISYLATE
    Application name
    ALPHARMA US PHARMS
    Application type
    A
    Application number
    087154
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    ALPHARMA US PHARMACEUTICALS DIVISION
    Dosage form
    SYRUP
    Route
    ORAL
    Active ingredients
    1. Name
      PROCHLORPERAZINE EDISYLATE
      Strength
      EQ 5MG BASE/5ML
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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.