Development and Validation of UV Spectrophotometric and Hptlc Methods for Simultaneous Estimation of Tapentadol Hydrochloride and Paracetamol in their Combined Dosage Form

By: Material type: FilmFilmPublication details: Ahmedabad Institute of Pharmacy, Nirma University 2013Description: 113pSubject(s): DDC 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 PDR00241-1
Dissertation Dissertation NIMA Knowledge Centre Reference 615.1901 SHA (Browse shelf(Opens below)) Not For Loan PDR00241
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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 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 615.1901 SHA Dissolution Method Development for Combined Dosage form of Amlodipine Besylate and Atenolol by Spectrophotometric Analysis

Guided by Dr. Priti J. Mehta

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