USFDA gives nod for this Blood Pressure injection

Norepinephrine Bitartrate Injection USP, 4 mg/4 mL (1 mg/mL) single-dose vial.

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USFDA Approval
USFDA Approval

Last Updated on October 11, 2024 by The Health Master

Ahmedabad: Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (USFDA) to market Norepinephrine Bitartrate Injection USP, 4 mg/4 mL (1 mg/mL) single-dose vial.

Norepinephrine bitartrate is indicated for the restoration of blood pressure in adult patients with acute hypotensive states.

The drug will be manufactured at the group’s topical injectable manufacturing facility at Jarod, India.

Norepinephrine Bitartrate Injection USP, 1 mg/1 mL had an annual sales of US$ 63.8 million in the United States according to IQVIA data.

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