Product NDC: | 0409-4348 |
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) |
Product NDC: | 0409-4348 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075955 |
Marketing Category: | ANDA |
Start Marketing Date: | 20021018 |
Package NDC: | 0409-4348-35 |
Package Description: | 2 TRAY in 1 PACKAGE (0409-4348-35) > 5 AMPULE in 1 TRAY > 3 mL in 1 AMPULE |
NDC Code | 0409-4348-35 |
Proprietary Name | Amiodarone Hydrochloride |
Package Description | 2 TRAY in 1 PACKAGE (0409-4348-35) > 5 AMPULE in 1 TRAY > 3 mL in 1 AMPULE |
Product NDC | 0409-4348 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | AMIODARONE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20021018 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | AMIODARONE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Antiarrhythmic [EPC] |