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DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF ASSAY AND CHROMATOGRAPHIC PURITY OF PARACETAMOL AND TRAMADOL HYDROCHLORIDE IN COMBINE FORM IN BULK DRUG AND PHARMACEUTICAL DOSAGE FORM BY HPCL AND UV

By:

KRUPA D. SHAH

Material type: Text

Text

TextPublication details: SUMANDEEP VIDYAPEETH PIPARIA 2014-2015Description: 94Subject(s):

DDC classification:

615.19

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Item type	Current library	Collection	Call number	Status	Date due	Barcode
DISSERTATION	Learning Resource Center - Sumandeep Vidyapeeth	PHARMACY DISSERTATION	615.19 (Browse shelf(Opens below))	Not for loan		PHD36410

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Previous	615.19 DEVELOPMENT AND VALIDATION OF RP-HPCL METHOD FOR ESTIMATION OF ROFLUMILAST AND ITS RELATED SUBSTANCES	615.19 DEVELOPMENT AND VALIDATION OF STABILITY INDICATING METHOD FOR THE DETERMINATION OF ASSAY AND CHROMATOGRAPHIC PURITY OF CEFTRIAXONE FOR INJECTION USP IN BULK DRUG AND PHARMACEUTICAL DOSAGE FORM BY RE-HPCL	615.19 VALIDATION OF HEATING VENTILATION AIR CONDITIONING SYSTEM AND WATER TRATMENT SYSTEM IN PHARMACEUTICAL INDUSTRY	615.19 DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF ASSAY AND CHROMATOGRAPHIC PURITY OF PARACETAMOL AND TRAMADOL HYDROCHLORIDE IN COMBINE FORM IN BULK DRUG AND PHARMACEUTICAL DOSAGE FORM BY HPCL AND UV	615.19 FORMULATION AND EVALUATION OF SUSTAINED RELEASE CHOLORHEXIDINE IN SITU GEL FOR PERIODONTITIS	615.19 DEASIGN DEVELOPMENT OPTIMIZATION AND CHARACTERIZATION OF ACECLOFENAC LOADED ETHOSOME FOR TRANSDERMAL DELIVERY	615.19 FORMULATION AND EVALUATION OF MUCOADHESIVE DRY SUSPENSION OF AZITHROMYCIN FOR PEDIATRICS USE	Next

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