Analysis Note
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Application
This USP reference standard is intended for use in specified quality tests and assays as specified in the USP compendia.It is also used in the preparation of standard solution for the analysis of organic impurities in tablets and capsules, in accordance with the USP monographs, by liquid chromatography (LC) combined with UV detection, such as the following: Amlodipine and benazepril hydrochloride capsules Amlodipine and valsartan tablets Amlodipine, valsartan, and hydrochlorothiazide tablets Amlodipine and olmesartan medoxomil tablets Amlodipine and atorvastatin tabletsIn addition, it is used in the assay test of amlodipine besylate tablets by LC-UV following the USP monograph “Amlodipine Besylate Tablets”.
General description
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Other Notes
Sales restrictions may apply.
USP issued SDS can be found here.
This product has met the following criteria to qualify for the following awards: