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U.S. Department of Health and Human Services

FDA Application
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NDC Search Results on Active Ingredient: Vinblastine

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
VINBLASTINE SULFATE 63323-278-10  Fresenius Kabi USA, LLC  ANDA089515  HUMAN PRESCRIPTION DRUG  ANDA 

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