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SUMATRIPTAN SUCCINATE

SUMATRIPTAN SUCCINATE · EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML) · SOLUTION · SUBCUTANEOUS

ANDA200183HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
20130916
Product number
001
Products
  1. Brand name
    SUMATRIPTAN SUCCINATE
    Application name
    HIKMA
    Application type
    A
    Application number
    200183
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    HIKMA FARMACEUTICA PORTUGAL SA
    Dosage form
    SOLUTION
    Route
    SUBCUTANEOUS
    Active ingredients
    1. Name
      SUMATRIPTAN SUCCINATE
      Strength
      EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
    Therapeutic equivalence codes
    AP
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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.