Zidovudine

Zidovudine Impurities & Reference Standards

Zidovudine is an established active pharmaceutical ingredient (API) with broad application in pharmaceutical formulation, drug substance manufacturing, and quality control. Zidovudine related substances / impurity reference standards support HPLC method validation, forced degradation studies, and regulatory documentation consistent with ICH, USP, BP, and EP requirements. We offer Zidovudine and its impurity standards with complete analytical documentation, including CoA and HPLC data, suitable for pharmaceutical quality control and regulatory submissions.