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
What is the diffeence between assay and uniformity of content
What is Delay & Dead Volume
What is the difference between chromatographic purity and related substances?
If vendor having more imp than monograph then how to proceed? and how to set spec?
In acid base titration, after complet consumption of HCl by NaOH, addition of next drop of NaOH will give pink colour with phenolpthalein indicator. Why this pink colour appear? Why not blue, black, green or anything elese?
how many types of Proceing methods?
what is the differance between Analytical and semi micro balance?
if you have given one product then how you determine the impurity in that?
Why we have to take 42gm of sodium hydroxide instead of 40gm for preparation of 1M Sodium hydroxide as per Pharmacopia? Whether it means the formula for calculating molarity was wrong?
5 Answers Claris Otsuka, Ranbaxy,
how we do assay of urea, ammonium sulpate, ammonium nitro pospate etc
what is the need of calulation of RRF of impurity in HPLC analysis?
IN DISSOLUTION S1 STAGE 1 BOWL GOT 52%(Q POINT IS 80%)WHAT WE HAVE DO