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
| Packaging sizes (GTIN) | Additional packaging sizes | Status | Date Created | Date Updated | Reports |
|---|---|---|---|---|---|
| No GTINs available | 3 mL | Resolved | 2023-06-14 | 2023-07-20 | 194926 |
| No GTINs available | 3 mL | Resolved | 2024-07-02 | 2024-08-30 | 231738 |
| No GTINs available | 50 mg/mL, MD Vial 3 mL | Resolved | 2020-03-19 | 2020-04-09 | 109070 |
| No GTINs available | 50 mg/mL, MD Vial 3 mL | Resolved | 2020-07-06 | 2020-08-06 | 119581 |
| No GTINs available | 3 mL | Resolved | 2022-09-01 | 2023-04-05 | 168496 |
Showing 1 to 5 of 5
Discontinuation reports
| Packaging sizes (GTIN) | Additional packaging sizes | Status | Date Created | Date Updated | Reports |
|---|
Showing 1 to 0 of 0