Development and validation of stability indicating RP-HPLC method for the simultaneous estimation of Sofosbuvir and Ledipasvir in bulk and their combined dosage form
Objective: A simple, specific, accurate and economic reverse phase liquid chromatographic method was developed for the simultaneous estimation of Sofosbuvir and Ledipasvir in bulk and tablet dosage form. Method: The method has shown adequate separation of Sofosbuvir and Ledipasvir from their degrada...
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| Autori principali: | , , , |
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| Natura: | Libro |
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SpringerOpen,
2018-12-01T00:00:00Z.
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| Collocazione: |
A1234.567 |
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| Copia 1 | Disponibile |