Development and Validation of UV Spectrophotometric and Stability Indicating RP-HPLC Assay Method for Agomelatine in Bulk and Pharmaceutical Formulations

By: Material type: FilmFilmPublication details: Ahmedabad Institute of Pharmacy, Nirma University 2012Description: 109pDDC classification:
  • 615.1901 SHA
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CD/DVD CD/DVD NIMA Knowledge Centre Reference 615.1901 SHA (Browse shelf(Opens below)) Not For Loan Dissertation CD PDR00186-1
Dissertation Dissertation NIMA Knowledge Centre Reference 615.1901 SHA (Browse shelf(Opens below)) Not For Loan PDR00186
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615.1901 SHA Development and Validation of UV Spectrophotometric, HPLC and RP-HPLC Methods for Simultaneous Estimation of Amlodipline Besylate. Hydrochlorothiazide and Valsartan in their Combined Tablet Dosage Form 615.1901 SHA Development and Validation of UV Spectrophotometric, HPLC and RP-HPLC Methods for Simultaneous Estimation of Amlodipline Besylate. Hydrochlorothiazide and Valsartan in their Combined Tablet Dosage Form 615.1901 SHA Development and Validation of UV Spectrophotometric and Stability Indicating RP-HPLC Assay Method for Agomelatine in Bulk and Pharmaceutical Formulations 615.1901 SHA Development and Validation of UV Spectrophotometric and Stability Indicating RP-HPLC Assay Method for Agomelatine in Bulk and Pharmaceutical Formulations 615.1901 SHA Development and Validation of UV Spectrophotometric and Hptlc Methods for Simultaneous Estimation of Tapentadol Hydrochloride and Paracetamol in their Combined Dosage Form 615.1901 SHA Development and Validation of UV Spectrophotometric and Hptlc Methods for Simultaneous Estimation of Tapentadol Hydrochloride and Paracetamol in their Combined Dosage Form 615.1901 SHA Development and Validation of Spectrophotometric and RP-HPLC for Simultaneous Estimation of Olanzapine and Fluoxetine Hydrochloride in Combined Dosage Form

Guided by Dr. Priti J. Mehta Industrial Guide: Mr. VIjendrasignh

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