Interested to Buy Any Domain ? << Click Here >> for more details...
What is the Deference between Bulk density & Tap density ?
- 2 Answers
- 25526 Views
- Hikma Pharmaceuticals, Neuland, Reddy Labs, I also Faced
- E-Mail Answers
Answer Posted / spln
Bulk Density (0 taps or Untapped): As is volume in
g/ml.This is called as apparent volume.
Tapped Density: after tapping only we can measure the qty
as g/ml. As per USP two types of methods is there, Method-
I&II.
Based on the powder nature tapping are fixed.500 taps, 750
taps & 1250 taps.(Varience% is NMT 2%)
Naturally all powder grades are fixed in 1250 taps.
After 1250taps also varience is more, then go to USP-II
method or any customer requirement is there then we can use
Method-II.
| Is This Answer Correct ? | 18 Yes | 2 No |
Post New Answer View All Answers
if rsd failed then what require to do?
how require to set assay concentration for standard and sample?
for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
WHY given much noise PDA dector then VWD Dector
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
How to choose the which salt is suitable for mobilephase
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
using gradient pressure in gas chromatography are not ?using gradient pressure why
what is partion and column chromatography
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
Why dissolution test is not performed in all of the products
