Načítá se...

A Fast, Stability-Indicating, and Validated Liquid Chromatography Method for the Purity Control of Lercanidipine Hydrochloride in Tablet Dosage Form

A robust, sensitive, and stability-indicating rapid resolution liquid chromatography method for the simultaneous determination of process impurities and degradation products of lercanidipine hydrochloride in pharmaceutical dosage form was developed and validated. The chromatographic separation was p...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Mehta, Saumil, Singh, Sukhdev, Chikhalia, Kishor
Médium: Artigo
Jazyk:Inglês
Vydáno: Österreichische Apotheker-Verlagsgesellschaft 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4065126/
https://ncbi.nlm.nih.gov/pubmed/24959405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3797/scipharm.1310-10
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!