FDA Application
-
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 |
-