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U.S. Department of Health and Human Services

FDA Application

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NDC Search Results on Active Ingredient: Amiodarone

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
AMIODARONE HYDROCHLORIDE 68382-227-06  Zydus Pharmaceuticals USA Inc.  ANDA079029  HUMAN PRESCRIPTION DRUG  ANDA 
AMIODARONE HYDROCHLORIDE 68382-227-14  Zydus Pharmaceuticals USA Inc.  ANDA079029  HUMAN PRESCRIPTION DRUG  ANDA 
AMIODARONE HYDROCHLORIDE 68382-227-10  Zydus Pharmaceuticals USA Inc.  ANDA079029  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-153

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