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 ...

To date, the Company has not received reports of any adverse events related to this recall. Fresenius Kabi is voluntarily recalling 7 lots of Sodium Acetate Injection, USP, 400mEq/100mL (4mEq/mL), ...

(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 ...

MINNETONKA, Minn.--(BUSINESS WIRE)--Milla Pharmaceuticals Inc., an A.forall company, announced that its partner, Woodward Pharma Services LLC, has just commercialized its Supplemental Abbreviated New ...

MINNETONKA, Minn.--(BUSINESS WIRE)--Milla Pharmaceuticals, a subsidiary of the Alter Pharma Group, announced that it has received abbreviated new drug application (ANDA) approval from the U.S. Food ...

Finding particulate matter in vials of Sodium Acetate Injection caused Chicago-area company Fresenius Kabi to recall seven lots of the sodium additive. Sodium Acetate Injection, USP, 400 mEq/100 mL (4 ...

Through its U.S. subsidiary, Milla Pharmaceuticals Inc., A.forall announced the direct commercialization and launch of Sodium Acetate Injection 2mEq/mL in 20mL, 50mL, and 100mL vials. Sodium Acetate ...

The full CMI on the next page has more details. If you are worried about using this medicine, speak to your doctor or pharmacist. 1. Why am I being treated with DBL Sodium Acetate Concentrated ...

Twelve solutions made at Pfizer’s Rocky Mount, N.C., facility — which a tornado struck in July — must now be ordered directly from the drugmaker’s emergency ordering system, according to an Aug. 3 ...