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 3 mL Resolved 2023-06-14 2023-07-20 194926
AMIODARONE HYDROCHLORIDE FOR INJECTION, USP 3 mL Resolved 2022-09-01 2023-04-05 168496
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 50 mg/mL, MD Vial 3 mL Resolved 2020-03-19 2020-04-09 109070

Showing 1 to 4 of 4

Discontinuation reports
Brand name Packaging Size Status Date Created Date Updated Reports

Showing 1 to 0 of 0