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Looking for 98243-58-4 / Verticillatine API manufacturers, exporters & distributors?

Verticillatine manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Verticillatine 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 Verticillatine manufacturer or Verticillatine supplier for your needs.

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

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

API | Excipient name

Verticillatine

Synonyms

98243-58-4, Verticillatine (rauwolfia), Dtxsid70913355, 18-norsarpaganium, 17,19-epoxy-19,20-dihydro-10,17-dihydroxy-4,21-dimethyl-, (20beta)-

Cas Number

98243-58-4

Verticillatine Manufacturers

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

Verticillatine Suppliers

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

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

Verticillatine USDMF

A Verticillatine DMF (Drug Master File) is a document detailing the whole manufacturing process of Verticillatine active pharmaceutical ingredient (API) in detail. Different forms of Verticillatine DMFs exist exist since differing nations have different regulations, such as Verticillatine USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Verticillatine DMF submitted to regulatory agencies in the US is known as a USDMF. Verticillatine USDMF includes data on Verticillatine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Verticillatine USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Verticillatine suppliers with USDMF on PharmaCompass.

Verticillatine GMP

Verticillatine 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 Verticillatine 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 Verticillatine GMP manufacturer or Verticillatine GMP API supplier for your needs.

Verticillatine CoA

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

Verticillatine CoA mostly includes findings from lab analyses of a specific batch. For each Verticillatine 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.

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