Brand(s): Sodium Chloride Injection Hypertonic, Baxter Injection, for 2.5 mEq of Sodium Chloride Additive preparation of Na+/mL and Solution, Abraxis IV admixtures Cl-/mL pharmacy bulk package 4 mEq ...

Sodium chloride injection is fundamental for clinicians in fluid resuscitation, medication delivery, and renal replacement. It necessitates a balance between clinical requirements and manufacturing ...

LAKE ZURICH, Ill.--(BUSINESS WIRE)--Fresenius Kabi announced today it has introduced two new presentations of Calcium Gluconate in Sodium Chloride Injection in the United States in the company’s ...

BETHLEHEM, Pa., July 18, 2025 /PRNewswire/ -- B. Braun Medical Inc. (B. Braun), a leader in smart infusion therapy and pain management, announced today the launch of its new Heparin Sodium Injections ...

Long Grove Pharmaceuticals is set to introduce Sodium Bicarbonate Injection. The product is commonly used in critical care settings yet routinely found on the drug shortages list, the company said.

LAKE ZURICH, Ill.--(BUSINESS WIRE)--Fresenius Kabi announced today it has introduced in the United States two new presentations of Heparin Sodium in convenient, ready-to-administer Freeflex ® IV bags.

ELMWOOD PARK, N.J., Nov. 4, 2025 /PRNewswire/ -- Glenmark Pharmaceuticals Inc., USA (Glenmark) is pleased to announce the upcoming launch1 of 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL (1 mEq ...

Hikma has launched sodium acetate injection in 40 mEq per 20 mL vials in the United States. The product was approved with a Competitive Generic Therapy designation from the Food and Drug ...

Exela Pharma Sciences is recalling an additional 14 lots of Sodium Bicarbonate Injection, USP, 8.4%, 50mEq/50 mL vial, 20-count carton. In total, the Company is recalling 63 lots of the product due to ...

Exela Pharma Sciences, LLC has voluntarily recalled 49 lots of Sodium Bicarbonate Injection, USP, 8.4%, 50mEq/50 mL vial, 20-count carton, due to a potential safety concern with vial breakage and ...

(RTTNews) - Fresenius Kabi USA is recalling seven lots of Sodium Acetate Injection, USP to the user level due to the presence of particulate matter, the US. Food and Drug Administration said. The ...