The manufacturer of cyclophosphamide involves several stages, each of which must be carefully monitored to ensure the drug’s purity and potency. The process begins with the synthesis of the active pharmaceutical ingredient (API), which is the chemical compound responsible for the drug’s therapeutic effects. This is followed by the formulation of the drug, where the API is combined with other ingredients to create a stable and effective product.
Once the drug is formulated, it undergoes rigorous testing to ensure it meets the required quality standards. This includes testing for purity, potency, and stability. After passing these tests, the drug is packaged and distributed to hospitals, pharmacies, and other healthcare facilities where it can be administered to patients.