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Combined Dosage Pharmaceutical Formulation

Simultaneous Determination and Validation of Ofloxacin and Ornidazole in Combined Dosage Pharmaceutical Formulation by RP-HPLC Method

Simultaneous Determination and Validation of Ofloxacin and Ornidazole in Combined Dosage Pharmaceutical Formulation by RP-HPLC Method

... The method was determined for simultaneous determination of ofloxacin and ornidazole from combined dosage form. The separation of drug was achieved on Zorbax Eclipse C18 (250 x 4.6 mm i.d.) with 5 µ ...

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STABILITY INDICATING ASSAY METHOD DEVELOPMENT AND VALIDATION FOR NEBIVOLOL AND TELMISARTAN IN ITS COMBINED PHARMACEUTICAL DOSAGE FORM

STABILITY INDICATING ASSAY METHOD DEVELOPMENT AND VALIDATION FOR NEBIVOLOL AND TELMISARTAN IN ITS COMBINED PHARMACEUTICAL DOSAGE FORM

... Based on the results of the above studies, it is concluded that the method for determination of assay of Nebivolol and Telmisartan is precise, linear over the concentration range, stability indicating, and robust. The ...

11

Simultaneous RP HPLC determination of Latanoprost and Timolol Maleate
in combined pharmaceutical dosage form

Simultaneous RP HPLC determination of Latanoprost and Timolol Maleate in combined pharmaceutical dosage form

... To study accuracy of the method, recovery experiment was carried out by applying the standard addition method. A known quantity of drug substance corresponding to 100%, 110%, 120% and 130% of the label claim of drug were ...

7

Development and Validation of RP-HPLC Method for Simultaneous Estimation of Metformin and 
      Linagliptin in Combined Pharmaceutical Dosage Form

Development and Validation of RP-HPLC Method for Simultaneous Estimation of Metformin and Linagliptin in Combined Pharmaceutical Dosage Form

... commercial formulation, 20 tablets of Metformin 500mg and Linagliptin ...of formulation solution were prepared and injected intlo HPLC to obtain concentration in linearity ...

5

METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF LYCOPENE AND UBIDECARENONE BY RP-HPLC IN COMBINED PHARMACEUTICAL DOSAGE FORM

METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF LYCOPENE AND UBIDECARENONE BY RP-HPLC IN COMBINED PHARMACEUTICAL DOSAGE FORM

... Methanol HPLC Grade, Tetrahydrofuran HPLC Grade, Acetonitrile HPLC Grade, Water HPLC Grade, and Ethanol HPLC Grade were used. The standard samples of Lycopene and Ubidecarenone were obtained as gift samples from Sai ...

6

“FORMULATION AND EVALUATION OF EXTENDED RELEASE DOSAGE FORM OF METFORMIN HYDROCHLORIDE USING A COMBINED HYDROPHOBIC AND HYDOPHILIC MATRIX: RATE OF IN-VITRO AND IN-VIVO RELEASE STUDIES” by K. Sundaramoorthy* and S. Kavimani, India.

“FORMULATION AND EVALUATION OF EXTENDED RELEASE DOSAGE FORM OF METFORMIN HYDROCHLORIDE USING A COMBINED HYDROPHOBIC AND HYDOPHILIC MATRIX: RATE OF IN-VITRO AND IN-VIVO RELEASE STUDIES” by K. Sundaramoorthy* and S. Kavimani, India.

... Metformin hydrochloride – USP was a gift sample from wockhard pharmaceuticals (Mumbai, India), hydroxyl propyl methyl cellulose (HPMC K100M) USP was obtained from shin-etsu, Chemicals Co.Ltd., (Tokyo, Japan). Ethyl ...

9

SIMULTANEOUS ESTIMATION OF DICLOFENAC SODIUM AND TOLPERISONE HYDROCHLORIDE IN COMBINED PHARMACEUTICAL FORMULATION

SIMULTANEOUS ESTIMATION OF DICLOFENAC SODIUM AND TOLPERISONE HYDROCHLORIDE IN COMBINED PHARMACEUTICAL FORMULATION

... Three simple, rapid, precise and accurate spectrophotometric methods have been developed for simultaneous analysis of Tolperisone Hydrochloride (TOL) and Diclofenac Sodium (DIC) in their combined dosage ...

6

High Performance Thin Layer Chromatographic determination of Cefixime and Ofloxacin in combined tablet dosage form

High Performance Thin Layer Chromatographic determination of Cefixime and Ofloxacin in combined tablet dosage form

... A new simple High Performance Thin Layer Chromatographic (HPTLC) method for determination of Cefixime and Ofloxacin in combined tablet dosage form has been developed and validated. The mobile phase selected ...

5

SPECTRUM SUBTRACTION METHOD FOR SIMULTANEOUS DETERMINATION OF PARACETAMOL AND ORPHENADRINE CITRATE IN THEIR COMBINED PHARMACEUTICAL DOSAGE FORMS

SPECTRUM SUBTRACTION METHOD FOR SIMULTANEOUS DETERMINATION OF PARACETAMOL AND ORPHENADRINE CITRATE IN THEIR COMBINED PHARMACEUTICAL DOSAGE FORMS

... The proposed method was successfully applied for determination of PAR and ORP in their pharmaceutical formulation (Orphenadrine plus® tablets). The results were acceptable and with sufficient agreement with ...

7

SIMULTANEOUS ESTIMATION OF RABEPRAZOLE SODIUM AND CINITAPRIDE HYDROGEN TARTRATE IN COMBINED PHARMACEUTICAL FORMULATION

SIMULTANEOUS ESTIMATION OF RABEPRAZOLE SODIUM AND CINITAPRIDE HYDROGEN TARTRATE IN COMBINED PHARMACEUTICAL FORMULATION

... ABSTRACT: Three simple, rapid, precise and accurate spectrophotometric methods have been developed for simultaneous analysis of Cinitapride Hydrogen Tartrate (CNT) and Rabeprazole Sodium (RAB) in their combined ...

6

Development and Validation of RP-HPLC Method for Simultaneous Estimation of Levosulpiride 
      and Pantoprazole in Combined Pharmaceutical Dosage Form

Development and Validation of RP-HPLC Method for Simultaneous Estimation of Levosulpiride and Pantoprazole in Combined Pharmaceutical Dosage Form

... ACCURACY:Accuracy is the closeness of results obtained by a method to the true value. It is the measure of exactness of the method. Recovery studies of the drug were carried out for determining accuracy parameter. ...

5

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD FOR THE ESTIMATION OF BICALUTAMIDE IN BULK AND PHARMACEUTICAL DOSAGE FORMS

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD FOR THE ESTIMATION OF BICALUTAMIDE IN BULK AND PHARMACEUTICAL DOSAGE FORMS

... A specific, accurate and precise Reverse Phase High Performance liquid chromatographic (RP-HPLC) method has been developed and validated for the estimation of bicalutamide in bulk and tablet dosage forms. A ...

11

SOLID STATE CRYSTALLINITY, AMORPHOUS STATE, AND ITS IMPLICATIONS IN THE PHARMACEUTICAL PROCESS

SOLID STATE CRYSTALLINITY, AMORPHOUS STATE, AND ITS IMPLICATIONS IN THE PHARMACEUTICAL PROCESS

... Many drugs exist in crystalline solid form due to reasons of stability and ease of handling during the various stages of drug development. Crystalline solids can exist in the form of polymorphs, solvates or hydrates. ...

11

“Spectrophotometric Quantitative Determination of Bromhexine Hydrochloride in Bulk and Pharmaceutical Dosage form using p-nitrobenzaldehyde Reagent” by K.Siddappa, Prashant C. Hanamshetty, India.

“Spectrophotometric Quantitative Determination of Bromhexine Hydrochloride in Bulk and Pharmaceutical Dosage form using p-nitrobenzaldehyde Reagent” by K.Siddappa, Prashant C. Hanamshetty, India.

... An efficient, sensitive spectrophotometric method has been developed and validated for the determination of Bromhexine hydrochloride (BRH), in bulk drug and its pharmaceutical formulations. The method is based on ...

6

PELLETS: AS PHARMACEUTICAL DOSAGE FORM

PELLETS: AS PHARMACEUTICAL DOSAGE FORM

...  Pelletization by extrusion and spheronization: The process involves first making the extrude from the powder material and then converting the extrudes into beads using the spheronizer. The powder material could be any ...

6

Simultaneous estimation of esomeprazole and domperidone by UV spectrophotometric method

Simultaneous estimation of esomeprazole and domperidone by UV spectrophotometric method

... The proposed method for simultaneous estimation of ESO and DOM in combined sample solutions was found to be simple, accurate and reproducible. Beer’s law was obeyed in the concentration range of 5-20 μg/ml and ...

5

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD FOR THE DETERMINATION OF TORSEMIDE IN BULK DOSAGE FORM AND PHARMACEUTICAL FORMULATION

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD FOR THE DETERMINATION OF TORSEMIDE IN BULK DOSAGE FORM AND PHARMACEUTICAL FORMULATION

... In order to develop a RP-HPLC method effective most of the effort should be spent in method development and optimization as this will improve the final method performance. A well developed method should be easy to ...

6

Estimation of olopatadine hydrochloride by RP–HPLC and U.V spectrophotometry  method in pure and pharmaceutical formulation

Estimation of olopatadine hydrochloride by RP–HPLC and U.V spectrophotometry method in pure and pharmaceutical formulation

... in pharmaceutical dosage form available in the market for ...Olopatadine pharmaceutical dosage form has been developed which can be employed in the industry for the routine ...

11

A simple and validated reverse phase HPLC method for the determination of Blonanserin in pharmaceutical dosage forms

A simple and validated reverse phase HPLC method for the determination of Blonanserin in pharmaceutical dosage forms

... suitability parameters were also calculated. To demonstrate specificity in the presence of excipients used in formulation, blonanserin was spiked in drug product; chromatogram was observed and compared with that ...

6

A NEW RP HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF ETODOLAC AND THIOCOLCHICOSIDE IN TABLET DOSAGE FORMS

A NEW RP HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF ETODOLAC AND THIOCOLCHICOSIDE IN TABLET DOSAGE FORMS

... mixture of acetate buffer (pH 3.7) and methanol (20:80 v/v) as the mobile phase at a flow rate of 0.8 mL/min. The analytes in the eluate were monitored at 242 nm. Under the optimized conditions, the retention times ...

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