Biorelevant Dissolution Method Development For Dutasteride/Tamsulosin Hydrochloride Modified Release Capsule - A Prognostic Tool For Oral Drug Absorption

Author:

Thamizhanban Devi,Tulja Rani Gampa,Krishnasamy Kathiresan, , ,

Publisher

Informatics Publishing Limited

Subject

General Pharmacology, Toxicology and Pharmaceutics

Reference14 articles.

1. Combination therapy with Dutasteride and Tamsulosin for the treatment of symptomatic enlarged prostate;Miller J, Tarter TH;Clinical Interventions in Aging.,2009

2. Center for Drug Evaluation and Research;US Food and Drug Administration;Printed Labelling for Jalyn (Dutasteride 0.5 mg/Tamsulosin hydrochloride 0.4 mg),2010

3. Wagner-Nelson and numerical deconvolution based approaches for in-vivo performance prediction;Rashee K;International Journal of Science and Research,2018

4. AAPS guidelines for dissolution/in vitro release testing of novel/special dosage forms;Siewert M, Dressman J, Brown C, Shah V;Dissolution Technologies,2003

5. Method development and validation for dissolution testings;Ramesh Babu B;Research Journal of Pharmaceutical, Biological and Chemical Sciences,2011

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