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Amiodarone HCl
Amiodarone HCl - 51862-156-30 - (Amiodarone Hydrochloride)
Drug Information of Amiodarone HCl
| Product NDC: | 51862-156 |
| Proprietary Name: | Amiodarone HCl |
| Non Proprietary Name: | Amiodarone Hydrochloride |
| Active Ingredient(s): | 400 mg/1 & nbsp; Amiodarone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amiodarone HCl
| Product NDC: | 51862-156 |
| Labeler Name: | Libertas Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077069 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130101 |
Package Information of Amiodarone HCl
| Package NDC: | 51862-156-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (51862-156-30) |
NDC Information of Amiodarone HCl
| NDC Code | 51862-156-30 |
| Proprietary Name | Amiodarone HCl |
| Package Description | 30 TABLET in 1 BOTTLE (51862-156-30) |
| Product NDC | 51862-156 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amiodarone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | ANDA |
| Labeler Name | Libertas Pharma, Inc. |
| Substance Name | AMIODARONE HYDROCHLORIDE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
