DEVELOPMENT AND VALIDATION OF A REVERSED-PHASE HPLC METHOD FOR ASSAY OF AZITHROMYCIN IN POWDER FOR ORAL SUSPENSION

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Conclusion
A simple, specific, linear, precise, accurate and stability indicating RP-HPLC method has been developed and validated for quantitative determination of azithromycin  in powder for oral suspension. Statistical analysis proves that method is repeatable and selective for the analysis of azithromycin in powder for oral suspension. As the method seperates the drug from its degradation products it can be employed as a stability indicating one. The developed method can be applicable for pharmaceutical dosage forms and in process testing.

References
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