Product NDC: | 0143-9875 |
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: | 0143-9875 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077234 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080225 |
Package NDC: | 0143-9875-10 |
Package Description: | 10 VIAL in 1 BOX (0143-9875-10) > 3 mL in 1 VIAL (0143-9875-01) |
NDC Code | 0143-9875-10 |
Proprietary Name | Amiodarone Hydrochloride |
Package Description | 10 VIAL in 1 BOX (0143-9875-10) > 3 mL in 1 VIAL (0143-9875-01) |
Product NDC | 0143-9875 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amiodarone Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20080225 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | AMIODARONE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Antiarrhythmic [EPC] |