Publication | Closed Access

Development of a stability-indicating UPLC method for determining olanzapine and its associated degradation products present in active pharmaceutical ingredients and pharmaceutical dosage forms

Medicinal ChemistryStability-indicating Uplc MethodPharmaceutical ScienceActive IngredientMedicineDrug PurityPharmaceutical Dosage FormsDegradation ProductsAnalytical ChemistryChromatographyPharmacologyPharmacokineticsDrug DiscoveryDrug Analysis