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Looking for 633-59-0 / Zuclopenthixol Hydrochloride API manufacturers, exporters & distributors?

Zuclopenthixol Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Zuclopenthixol Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zuclopenthixol Hydrochloride manufacturer or Zuclopenthixol Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zuclopenthixol Hydrochloride manufacturer or Zuclopenthixol Hydrochloride supplier.

PharmaCompass also assists you with knowing the Zuclopenthixol Hydrochloride API Price utilized in the formulation of products. Zuclopenthixol Hydrochloride API Price is not always fixed or binding as the Zuclopenthixol Hydrochloride Price is obtained through a variety of data sources. The Zuclopenthixol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Zuclopenthixol Hydrochloride

Synonyms

Mls002154089, Nsc329015, Nsc-329015, Smr001233397, Clopenthixol dihydrochloride, Chlorpenthixol dihydrochloride

Cas Number

633-59-0

Zuclopenthixol Dihydrochloride Manufacturers

A Zuclopenthixol Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zuclopenthixol Dihydrochloride, including repackagers and relabelers. The FDA regulates Zuclopenthixol Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zuclopenthixol Dihydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Zuclopenthixol Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Zuclopenthixol Dihydrochloride Suppliers

A Zuclopenthixol Dihydrochloride supplier is an individual or a company that provides Zuclopenthixol Dihydrochloride active pharmaceutical ingredient (API) or Zuclopenthixol Dihydrochloride finished formulations upon request. The Zuclopenthixol Dihydrochloride suppliers may include Zuclopenthixol Dihydrochloride API manufacturers, exporters, distributors and traders.

click here to find a list of Zuclopenthixol Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Zuclopenthixol Dihydrochloride GMP

Zuclopenthixol Dihydrochloride Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Zuclopenthixol Dihydrochloride GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Zuclopenthixol Dihydrochloride GMP manufacturer or Zuclopenthixol Dihydrochloride GMP API supplier for your needs.

Zuclopenthixol Dihydrochloride CoA

A Zuclopenthixol Dihydrochloride CoA (Certificate of Analysis) is a formal document that attests to Zuclopenthixol Dihydrochloride's compliance with Zuclopenthixol Dihydrochloride specifications and serves as a tool for batch-level quality control.

Zuclopenthixol Dihydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Zuclopenthixol Dihydrochloride CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Zuclopenthixol Dihydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Zuclopenthixol Dihydrochloride EP), Zuclopenthixol Dihydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zuclopenthixol Dihydrochloride USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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