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 |
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AMIODARONE HYDROCHLORIDE | 51672-4057-6 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 63739-051-10 | McKesson Corporation dba SKY Packaging | ANDA079029 | HUMAN PRESCRIPTION DRUG | ANDA |
AMIODARONE HYDROCHLORIDE | 71335-0881-1 | Bryant Ranch Prepack | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
1-30 | 31-60 | 61-90 | 91-120 | 121-150 | 151-153 |
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