Development and validation of a stability-indicating ultra-performance liquid chromatography (UPLC) method for doxycycline hyclate: an optimization of the analytical methodology for a medical countermeasure (MCM) drug
Author:
Affiliation:
1. Division of Product Quality Research
2. CDER
3. FDA
4. USA
5. OGROP/ORA/CE-FO-FDA-Detroit Lab
6. Detroit
7. Counter-Terrorism and Emergency Coordination Staff (CTECS)
Abstract
Doxycycline hyclate drug product impurities and rapid quantification using a validated UPLC method.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Engineering,General Chemical Engineering,Analytical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/AY/C8AY00078F
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3. Doxycycline
4. Consideration for Improvement of Demetia that Uses Communications
5. Guidelines for Treatment of Anthrax
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