in dissolution in one tablets two molecule one is losartan &
second is HCTZ
losartam is complies in s1 stage & hctz is complies in s2
stage
then how to report result
losartan s1 stage result or losartan s2 stage result
Answer Posted / jignesh
Losartan in S1 stage and HCTZ in S2 stage.
Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
What is the difference between chromatographic purity and related substances?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
what is classification of elemental impurities? what is risk assement in elemental impurities?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
about method developement in hplc
what is definition of validation? which components are followed give detail?
how you determine moist.of NaOH sol or NaOH flacks
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
As per ICH related substances stability trend limit from initial to shelf life
mahagenco syllabus for the post of chemist
what is mean by covalidation