News

Fresenius Kabi has announced another voluntary recall of a single lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200mcg/50mL, 50mL fill in a 50mL vial due to the possibility of ...
The product is packaged as Sodium Chloride Injection, USP 0.9%, 10mL fill in a 10mL vial; Sodium Chloride Injection, USP 0.9% 20mL fill in a 20mL vial; both size vials are packaged in a 25-unit tray.
The 2 recalled lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, NDC Number 63323-671-50, include: Batch Number 6121853; Expiration Date 05/2021; Distributed between 6/3/2019 and 12/4 ...
Single-dose ADD-Vantage, conventional vial, and frozen bag formulations supplied as 3.375- and 4.5-g doses were utilized for intermittent infusion. Piperacillin-tazobactam in 0.9% sodium chloride ...
Nexus Pharmaceuticals has received the Food and Drug Administration’s green light for 0.9% sodium chloride injection, in 10 ml and 20 ml single-dose vials. “This product is part of an ...
Hospira is voluntarily recalling sodium bicarbonate and succinylcholine chloride vials that had microbial growth and were susceptible to contamination, which could cause sepsis, the U.S. Food and ...
Find patient medical information for Saline (Sodium Chloride) for Nebulization on WebMD including its uses, side effects and safety, interactions, pictures, warnings, and user ratings ...
Sterile 0.9% Sodium Chloride Injection, USP is added to dilute the child's COVID vaccines. It's a necessary step in preparing a dose. Next, he or she adds the sodium chloride to the vial, to ...
Labetalol HCl injection, 100 mg/20 ml and 200 mg/40 ml vial had a market value of approximately $6 million in the 12 months ended March 2021, according to IQVIA.
In August, Baxter recalled a single lot of 0.9% sodium chloride injection, in 1000-mL bags, after particulate matter was found near the administration port in some containers.
As part of the action, 42 lots of sodium bicarbonate vials were recalled along with five lots of succinylcholine chloride. Hospira said it is unaware of any reports of adverse events associated ...