Crisaborole API

Name：Crisaborole

CAS:906673-24-3

MF:C14H10BNO3

MW:251.05

EINECS:250-635-4

MDL No.:MFCD17169940

Properties

Melting point:>130°C (softened)

Boiling point:425.9±55.0 °C(Predicted)

Density 1.33±0.1 g/cm3(Predicted)

storage temp. room temp

solubility DMSO (Slightly), Methanol (Slightly)

form powder

pka7.00±0.20(Predicted)

color white to beige

Stability:Hygroscopic

Crisaborole API pharmaceutical export

Crisaborole API pharmaceutical wholesaler

Shortage Crisaborole API Supplies

supply of various Crisaborole API

Crisaborole API Import and Export Wholesaler

wholesale distribution of Crisaborole API

Crisaborole API DISTRIBUTION CHANNELS

Wholesaler Distributor Licensure of Crisaborole API

Certificate of Analysis (COA) for Crisaborole API

Valid Crisaborole API GMP certification

Valid Crisaborole API Manufacturing License

Method of Analysis for Crisaborole API

Material safety data sheet for Crisaborole API

Accelerated stability data for Crisaborole API

Real time stability data for Crisaborole API

Crisaborole API Exporters and Contract manufacturing

Crisaborole in USP, BP, EP with DMF, Tech Pack, GMP, Written Confirmation

Regulatory Documents of Crisaborole

Crisaborole  API of manufacturers who are USFDA audited & accredited with GMP, ISO

Crisaborole with DMF/GMP/ISO (all technical documents support)

Crisaborole  API in USP/BP/EP pharmacopoeia

Crisaborole  Micronised, Injection, & all grades

Crisaborole  API factory accredited by USFDA, Health Canada, TGA, UK-MHRA, PIC/S

Crisaborole  API with cGMP manufacturing facility、GMP certified facility

Crisaborole  API with GLP certified laboratory

Crisaborole  API with cGMP & WHO GMP compliant facility

Crisaborole  API with R&D and Commercial quantity

Dosage form of Crisaborole  API

Crisaborole  API U.sPharmacopeia (UsP), in-house specification and/or European Pharmacopoeia (Ph. Eur) 

Crisaborole  API distributor with a strong supply chain channel

Crisaborole  API Provide CEP/COS(certificate of suitability to monograph of European Pharmacopoeia)  , EDMF(European Drug Master File),and GMP(Good Manufacturing Practice ),Written Confirmation.

Crisaborole  API certificate of analysis

Crisaborole  API factory GMP (Goods Manufacturing Practices Certificate ) 

Crisaborole  API Product DML (Drug Manufacturing License)

    TOSUN PHARM was established in 1999. In China, it is a collection of drugs, APIs, reference listed drugs, impurities, excipients, intermediates import and export, import registration services, generic drug research and development services, innovative drugs and high-end FDF technology transfer, A group company integrating marketing, academic promotion and cooperative production. With a global procurement, R&D and marketing network, it can quickly meet the needs of product R&D, production and market sales of Chinese and global pharmaceutical companies.

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