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 | 51672-4025-2 | Taro Pharmaceuticals U.S.A., Inc. | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 67457-153-18 | Mylan Institutional LLC | ANDA076217 | 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 |
-
