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Amiodarone hydrochloride
Amiodarone hydrochloride - 21695-796-90 - (Amiodarone hydrochloride)
Drug Information of Amiodarone hydrochloride
| Product NDC: | 21695-796 |
| 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: | 21695-796 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079029 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090810 |
Package Information of Amiodarone hydrochloride
| Package NDC: | 21695-796-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-796-90) |
NDC Information of Amiodarone hydrochloride
| NDC Code | 21695-796-90 |
| Proprietary Name | Amiodarone hydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE (21695-796-90) |
| Product NDC | 21695-796 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amiodarone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090810 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | AMIODARONE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
