Forced degradation of flibanserin bulk drug: development and validation of stability indicating RP-HPLC method
Background: Flibanserin had been approved as the first drug by United State Food and Drug Administration (USFDA) for the treatment of female sexual interest/arousal disorder of any severity. However, the stability of this drug has yet to be studied extensively. Objectives: The objectives of this stu...
Saved in:
Main Authors: | Chew, Yik-Ling, Lee, Hon-Kent, Khor, Mei-Ann, Liew, Kai-Bin, Lokesh, Bontha Venkata Subrahmanya, Akowuah, Gabriel Akyirem |
---|---|
Format: | Article |
Published: |
Association of Pharmaceutical Teachers of India
2022
|
Subjects: | |
Online Access: | http://eprints.um.edu.my/42370/ |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
HPLC profile and antihyperglycemic effect of ethanol extracts
of Andrographis paniculata in normal and streptozotocin-induced diabetic rats
by: Ahmad, Mariam, et al.
Published: (2007) -
Stability-indicating RP-HPLC method for simultaneous quantitation of tramadol and aceclofenac in presence of their major degradation products: Method development and validation
by: ., Md. Gousuddin, et al.
Published: (2017) -
Determination of corticosteroids in Malay traditional jamu using RP-HPLC-PDA method
by: Yet, Lew Chin
Published: (2023) -
Development and validation of new RP-HPLC method
for the determination of gliclazide in tablet dosage form
by: Alaama, Mohamed, et al.
Published: (2017) -
Isocratic RP-HPLC Method for the Simultaneous Determination of Reaction Rate in N-phenylbenzamide Synthesis
by: Helal Uddin, A.B.M.
Published: (2021)