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NIZATIDINE

NIZATIDINE · 150MG · CAPSULE · ORAL

ANDA076178HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20020705
Product number
001
Products
  1. Brand name
    NIZATIDINE
    Application name
    EPIC PHARMA LLC
    Application type
    A
    Application number
    076178
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    EPIC PHARMA LLC
    Dosage form
    CAPSULE
    Route
    ORAL
    Active ingredients
    1. Name
      NIZATIDINE
      Strength
      150MG
    Therapeutic equivalence codes
    AB
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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.