Reports for AMIODARONE HYDROCHLORIDE FOR INJECTION, USP
Brand name
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP
Company Name
FRESENIUS KABI CANADA LTD
|
Drug Identification Number
02245248 |
Ingredients
AMIODARONE HYDROCHLORIDE |
Ingredient Strength
50 MG |
ATC Code
C01BD |
ATC Descriptor
ANTIARRHYTHMICS, CLASS I AND III |
Status
MARKETED
|
Shortage reports
Brand name | Packaging Size | Status | Date Created | Date Updated | Reports |
---|---|---|---|---|---|
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP | 50 mg/mL, MD Vial 3 mL | Resolved | 2020-03-19 | 2020-04-09 | 109070 |
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP | 50 mg/mL, MD Vial 3 mL | Resolved | 2020-07-06 | 2020-08-06 | 119581 |
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP | 3 mL | Resolved | 2022-09-01 | 2023-04-05 | 168496 |
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP | 3 mL | Resolved | 2023-06-14 | 2023-07-20 | 194926 |
Showing 1 to 4 of 4
Discontinuation reports
Brand name | Packaging Size | Status | Date Created | Date Updated | Reports |
---|
Showing 1 to 0 of 0