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METHYLPREDNISOLONE SODIUM SUCCINATE

METHYLPREDNISOLONE SODIUM SUCCINATE · EQ 500MG BASE/VIAL · INJECTABLE · INJECTION

ANDA081267DISCONTINUED
Open FDA's page for this record
Approval date
19921130
Product number
001
Products
  1. Brand name
    METHYLPREDNISOLONE SODIUM SUCCINATE
    Application name
    TEVA PARENTERAL
    Application type
    A
    Application number
    081267
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    DISCONTINUED
    Application full name
    TEVA PARENTERAL MEDICINES INC
    Dosage form
    INJECTABLE
    Route
    INJECTION
    Active ingredients
    1. Name
      METHYLPREDNISOLONE SODIUM SUCCINATE
      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.