Search Results - Mantena, Bhaskara P.V.

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  1. 1
    Development and Validation of RP-UPLC Method for the Determination of Process and Degradant Impurities Present in Dabigatran Etexilate Mesylate Capsules Using High Strength Silica-T3 Sorbent Column

    Development and Validation of RP-UPLC Method for the Determination of Process and Degradant Impurities Present in Dabigatran Etexilate Mesylate Capsules Using High Strength Silica-... by Mantena, Bhaskara P.V, Rao, Sumathi V, Suryakala, D., Ramakrishna, K., Srikanth Reddy, R

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  2. 2
    In vitro Dissolution Method for Alendronate Sodium and Vitamin D3 Tablets Using HPLC with Combination of Refractive Index and Ultraviolet Detectors

    In vitro Dissolution Method for Alendronate Sodium and Vitamin D3 Tablets Using HPLC with Combination of Refractive Index and Ultraviolet Detectors by Murali Krishna, M.V.V.N., Rao, Sumathi V, Venugopal, N.V.S., Mantena, Bhaskara P.V

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  3. 3
    Simultaneous Determination of Acetaminophen and Tramadol Impurities in combination product of Acetaminophen and Tramadol Tablets by UPLC with Trifunctional Octadecyl Column

    Simultaneous Determination of Acetaminophen and Tramadol Impurities in combination product of Acetaminophen and Tramadol Tablets by UPLC with Trifunctional Octadecyl Column by Murali Krishna, M.V.V.N., Rao, Sumathi V, Venugopal, N.V.S., Mantena, Bhaskara P.V

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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
    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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  6. 6
    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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  7. 7
    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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  8. 8
    Rapid Analytical Technique for the Quantification of Specified and Unspecified Impurities Present in Amlodipine besylate and Olmesartan medoxomil Fixed Dose Combination Drug Product Using Ethylene-Bridged RP-UPLC Column

    Rapid Analytical Technique for the Quantification of Specified and Unspecified Impurities Present in Amlodipine besylate and Olmesartan medoxomil Fixed Dose Combination Drug Produc... by Mantena, Bhaskara P.V., Rao, Sumathi V., Suryakala, D., Ramakrishna, K., Srikanth Reddy, R.

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  9. 9
    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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  10. 10
    Determination of Potential Impurities of Naproxen Sodium in Soft Gelatin Capsules Dosage by Using Ultra Performance Liquid Chromatography

    Determination of Potential Impurities of Naproxen Sodium in Soft Gelatin Capsules Dosage by Using Ultra Performance Liquid Chromatography by Reddy, R. Srikanth, Krishna, R. Murali, Vekaria, N.A., Sumathi, Rao V., Mantena, Bhaskara P.V.

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  11. 11
    Method Development and Validation for the Determination of Potential Impurities Present in Azilsartan medoxomil Tablets by Reverse Phase-Ultra Performance Liquid Chromatography

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

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