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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

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Material type: Film

FilmPublication details: Ahmedabad Institute of Pharmacy, Nirma University 2011Description: 109pSubject(s):

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Holdings
Item type	Current library	Collection	Call number	Status	Notes	Date due	Barcode	Item holds
CD/DVD	NIMA Knowledge Centre	Reference	615.1901 SHA (Browse shelf(Opens below))	Not For Loan	Dissertation CD		PDR00155-1
Dissertation	NIMA Knowledge Centre	Reference	615.1901 SHA (Browse shelf(Opens below))	Not For Loan			PDR00155

Total holds: 0

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Previous	615.1901 SHA Analytical Method Development of novel Anti-Hyperlipidaemic Agents in Combined Dosage Forms	615.1901 SHA Capillary Electrophoresis and Its Applications	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	Next

Guided by Dr. Charmi Kothari

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