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Amiodarone Hydrochloride
Amiodarone Hydrochloride - 63323-616-03 - (AMIODARONE HYDROCHLORIDE)
Drug Information of Amiodarone Hydrochloride
| Product NDC: | 63323-616 |
| Proprietary Name: | Amiodarone Hydrochloride |
| Non Proprietary Name: | AMIODARONE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/mL & nbsp; AMIODARONE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amiodarone Hydrochloride
| Product NDC: | 63323-616 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075761 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030128 |
Package Information of Amiodarone Hydrochloride
| Package NDC: | 63323-616-03 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-03) > 3 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Amiodarone Hydrochloride
| NDC Code | 63323-616-03 |
| Proprietary Name | Amiodarone Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-616-03) > 3 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-616 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMIODARONE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030128 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | AMIODARONE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
