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 | 72078-046-09 | Mylan Institutional LLC | ANDA076217 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 67457-153-18 | Mylan Institutional LLC | ANDA076217 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 67457-153-03 | Mylan Institutional LLC | ANDA076217 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 67457-153-09 | Mylan Institutional LLC | ANDA076217 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 67457-153-99 | Mylan Institutional LLC | ANDA076217 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 0615-8258-39 | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 0615-8258-05 | NCS HealthCare of KY, LLC dba Vangard Labs | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 21695-796-30 | Rebel Distributors Corp. | ANDA079029 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 21695-796-90 | Rebel Distributors Corp. | ANDA079029 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-1939-0 | REMEDYREPACK INC. | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-3439-1 | REMEDYREPACK INC. | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-3439-0 | REMEDYREPACK INC. | ANDA078578 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-1939-1 | REMEDYREPACK INC. | ANDA204742 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-2792-0 | REMEDYREPACK INC. | ANDA075761 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 70518-2792-1 | REMEDYREPACK INC. | ANDA075761 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 53808-1066-1 | State of Florida DOH Central Pharmacy | ANDA079029 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4025-3 | Taro Pharmaceuticals U.S.A., Inc. | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4056-1 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4057-6 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4025-4 | Taro Pharmaceuticals U.S.A., Inc. | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4056-6 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4057-0 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4056-3 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4055-6 | Taro Pharmaceuticals U.S.A., Inc. | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4056-0 | Taro Pharmaceuticals U.S.A., Inc. | ANDA076362 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 51672-4025-2 | Taro Pharmaceuticals U.S.A., Inc. | ANDA075424 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 29300-359-16 | Unichem Pharmaceuticals (USA), Inc. | ANDA213446 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 29300-359-05 | Unichem Pharmaceuticals (USA), Inc. | ANDA213446 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 0245-0147-01 | Upsher-Smith Laboratories, LLC | ANDA075135 | HUMAN PRESCRIPTION DRUG | ANDA |
| AMIODARONE HYDROCHLORIDE | 0245-1645-89 | Upsher-Smith Laboratories, LLC | ANDA075135 | HUMAN PRESCRIPTION DRUG | ANDA |
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