Zydus Lifesciences gets USFDA's final nod for Erythromycin Tablets

09 Mar 2023 Evaluate

Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) for Erythromycin Tablets USP, 250 mg and 500 mg (USRLD: Erythromycin Tablets). Erythromycin Tablets USP, 250 mg and 500 mg are used to prevent and treat infections in many different parts of the body, including respiratory tract infections, skin infections, diphtheria, intestinal amebiasis, acute pelvic inflammatory disease, legionnaire's disease, pertussis and syphilis.

The drugs will be manufactured at the group’s formulation manufacturing facility in Moraiya, Ahmedabad (India). Erythromycin Tablets USP, 250 mg and 500 mg had annual sales of $25.1 million in the United States (IQVIA MAT Dec. 2022). The group now has 350 approvals and has so far filed over 440 ANDAs since the commencement of the filing process in FY 2003-04.

Zydus Lifesciences (formerly known as Cadila Healthcare) is an India-based pharmaceutical company.

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