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Amiodarone Hydrochloride
Amiodarone Hydrochloride - 51672-4025-3 - (Amiodarone Hydrochloride)
Drug Information of Amiodarone Hydrochloride
| Product NDC: | 51672-4025 |
| Proprietary Name: | Amiodarone Hydrochloride |
| Non Proprietary Name: | Amiodarone Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Amiodarone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amiodarone Hydrochloride
| Product NDC: | 51672-4025 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075424 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010330 |
Package Information of Amiodarone Hydrochloride
| Package NDC: | 51672-4025-3 |
| Package Description: | 1000 TABLET in 1 BOTTLE (51672-4025-3) |
NDC Information of Amiodarone Hydrochloride
| NDC Code | 51672-4025-3 |
| Proprietary Name | Amiodarone Hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE (51672-4025-3) |
| Product NDC | 51672-4025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amiodarone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010330 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | AMIODARONE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
