Interested to Buy Any Domain ? << Click Here >> for more details...
What is the limit for friability of tablets?
- 10 Answers
- 56688 Views
- Glenmark, I also Faced
- E-Mail Answers
Answer Posted / aimsizer
Friability test limits is that if obviously cracked, cleaved, or broken tablets are present in the tablet sample after tumbling, the sample fails the test. If the results are doubtful or if the weight loss is greater than the targeted value, the test should be repeated twice and the mean of the three tests determined. A maximum mean weight loss from the three samples of not more than 1.0% is considered acceptable for most products. Conventional compressed tablets that lose less than 0.5% to 1% of weight are considered acceptable, less than 0.5% shows superior friability of tablets.
| Is This Answer Correct ? | 4 Yes | 4 No |
Post New Answer View All Answers
plzzz..send me the pevious papers of drug inspector for uppsc....i.l b highly oblige
If granules are over lubricated what defect arises in tablet compression how we solve this problem.
What steps would you take to ensure responsible prescribing and prevent overuse or misuse of Alprazolam in your patients?
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?
plzzz mail me question papers and syllabus of mpsc's and upsc's drug inspector's exam.and details whn da exm is going to be.. my e-mail id is shubhg_2007@yahoo.com.thanx..
what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
What is the difference between uniformity of content and content uniformity as official test for all tablets?
Discuss the potential side effects and risks associated with Alprazolam usage. How would you manage or mitigate these side effects in a patient?
why we use PG as a taxonomic marker ?
what we do when calibration of any instrument is fail ?
Why and When RRF is necessary in RS method? How it is helpful in method development?
hello,am milan mohite,i have completed B.PHARM,in 2008.and now do M.B.A from ignou,and D.P.P.M,from IPER{PUNE},please suggest me best coaching institute in pune for drug inspector,and send me model question paper for prepration of D.I. on my e.mail id - milan_mohite@yahoo.in Thanks.
if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration
What do you mean by Q+5 in dissolution?
