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Description

Please note: On August 1, 2018, USP posted a Compendial Notice for the Levodopa Capsules monograph. The monograph will be proposed for omission in Pharmacopeial Forum 44(5) [Sep-Oct 2018]. For the full Compendial Notice go to: https://www.uspnf.com/notices/levodopa-capsomission <br /> The monograph is anticipated to be omitted on December 1, 2019 in USP42-NF37 2nd Supplement if no comments of opposition are received. USP Levodopa Related Compound A RS future Lot R09510 was not tested and approved for use in the USP Levodopa Capsules monograph since the monograph is being proposed for omission. Lot R09510 is suitable for all other USP compendial uses. This lot is for qualitative use only as a system suitability standard.

Hazards

Harmful

Structure formula

3-(3,4,6-Trihydroxyphenyl)-alanine

Contents

Miscellaneous

Certificate of Analysis (specimen)

Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com

Product data sheet

View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information

Quality Solution Sheet (QSS)

A QSS is a resource for you integrating newly released reference standards and monographs with an overview of all relevant associated physical materials, PAIs, and soon: General Chapters, excipients, education, and other products and services. Get all the information you need at a glance.

USP | United States Pharmacopeia

US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.

Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.

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