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  1. 1
    Stability‐indicating RP‐HPLC method development and validation for the quantification of amlodipine besylate and valsartan tablets in solid oral dosage form

    Stability‐indicating RP‐HPLC method development and validation for the quantification of amlodipine besylate and valsartan tablets in solid oral dosage form von Kamireddy, Teja, Sambu, Pranitha, Lankalapalli, Prasanna Kumar, Myneni, Rama Krishna, Divadari, Hareesh

    Veröffentlicht in Biomedical chromatography

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  2. 2
    Development and Validation of LC-MS/MS Method for the Estimation of Lovastatin and its Metabolite (β-Hydroxy Acid) in Pharmaceutical Dosage Form

    Development and Validation of LC-MS/MS Method for the Estimation of Lovastatin and its Metabolite (β-Hydroxy Acid) in Pharmaceutical Dosage Form von Divadari, Hareesh, Pothula, Vijay Srinivas


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