Search Results - Mantena, Bhaskara P. V.

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  1. 1
    Method Development and Validation for the Determination of Potential Impurities Present in Olmesartan Medoxomil and Hydrochlorothiazide in Fixed Dose Combination Drug Product by Using Reverse Phase - Ultra-Performance Liquid Chromatography Coupled with Diode-Array Detector

    Method Development and Validation for the Determination of Potential Impurities Present in Olmesartan Medoxomil and Hydrochlorothiazide in Fixed Dose Combination Drug Product by Us... by Srikanth Reddy, R., Murali Krishna, R., Vekaria, N. A., Rao, Sumathi V., Mantena, Bhaskara P. V.

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  2. 2
    Method Development and Validation for the Determination of Four Potential Impurities Present in Darunavir Tablets by Reverse Phase-Ultra-Performance Liquid Chromatography Coupled with Diode-Array Detector

    Method Development and Validation for the Determination of Four Potential Impurities Present in Darunavir Tablets by Reverse Phase-Ultra-Performance Liquid Chromatography Coupled w... by Mantena, Bhaskara P. V., Rao, Sumathi V., Appa Rao, K. M. Ch, Ramakrishna, K., Reddy, R. Srikanth

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  3. 3
    Rapid Separation Technique for the Determination of Potential Impurities Present in Levodopa, Carbidopa, and Entacapone in Fixed Dose Combination Drug Product Using Trifunctionally Bonded Phase Ethylene Bridged Sorbent Column with Smaller Ion-Pair Reagent

    Rapid Separation Technique for the Determination of Potential Impurities Present in Levodopa, Carbidopa, and Entacapone in Fixed Dose Combination Drug Product Using Trifunctionally... by Mantena, Bhaskara P. V., Rao, Sumathi V., Rao, K. M. Ch. Appa, Ramakrishna, K., Reddy, R. Srikanth

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  4. 4
    Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method

    Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method by Mantripragada, Murali Krishna V V N, Rao, Sumathi V, Nutulapati, Venugopal V S, Mantena, Bhaskara P V

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  5. 5
    HPLC Method for Simultaneous Determination of Potential Impurities of Norgestimate and Ethinyl Estradiol in Combination Drug Product Using Sub-2 mu m Column

    HPLC Method for Simultaneous Determination of Potential Impurities of Norgestimate and Ethinyl Estradiol in Combination Drug Product Using Sub-2 mu m Column by Mantena, Bhaskara PV, Rao, Sumathi V, Rao, KMChAppa, Ramakrishna, K, Vittal, S P

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  6. 6
    HPLC Method for Simultaneous Determination of Potential Impurities of Norgestimate and Ethinyl Estradiol in Combination Drug Product Using Sub-2 µm Column

    HPLC Method for Simultaneous Determination of Potential Impurities of Norgestimate and Ethinyl Estradiol in Combination Drug Product Using Sub-2 µm Column by Mantena, Bhaskara P. V., Rao, Sumathi V., Rao, K. M. Ch. Appa, Ramakrishna, K., Vittal, S. P.

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