Levosimendan from Kinsy

KINSY is an independent chemical company, located in Murcia (Spain), having broad expertise in development, scale-up and commercial production of fine chemicals, with a strong focus on development and manufacturing of key pharmaceutical intermediates and APIs under cGMP.

Producer

Produced in:

Spain

MOQ: -

  • GMP

  • CoA

Contact supplier

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Kinsy Levosimendan API Producer - 141505-33-1

Description:
Kinsy offers high-quality Levosimendan API, certified for compliance with international standards. Manufactured in Spain.

Product Details

Certifications
GMP, CoA compliant
Minimum Order Quantity
Produced in
Spain (Europe)
DrugBank ID
DB00922
CAS Number
141505-33-1
Unique Ingredient Identifier
C6T4514L4E
Raw Material Category
Calcium regulators

Ordering Process

1. Inquiry Submission: Click "Send Inquiry" to connect directly with producer.

2. Requirement Specification: Outline your needs for tailored offers.

3. Quotation: Receive the best quote and terms exclusively through Pharmaoffer.

Quality Assurance

Kinsy has successfully passed audits conducted by Eurofins, with reports available that underscore the company's commitment to quality and transparency.

Additional Products

We offer 8 other Active Pharmaceutical Ingredients and excipients, showcasing our production and distribution capabilities.

Contact Us

Are you looking for Levosimendan API? Contact Kinsy by using the send inquiry button. We will respond quickly with pricing and terms exclusively through Pharmaoffer.

Please, provide enough information regarding your inquiry. Let us know whether you require Ph.Eur (EP), USP, BP, JP grade, whether you are looking for hydrochloride (HCl), base, or other specific product specifications. Additionally, please inform us if the API is intended for your own production, resale, or research purposes. Contact us to receive a quote, download certificates, and purchase the Levosimendan API

Kinsy


KINSY is an independent chemical company, located in Murcia (Spain), having broad expertise in development, scale-up and commercial production of fine chemicals, with a strong focus on development and manufacturing of key pharmaceutical intermediates and APIs under cGMP.