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Looking for 1982-37-2 / Methdilazine API manufacturers, exporters & distributors?

Methdilazine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Methdilazine

Synonyms

Tacaryl, 1982-37-2, Methdilazinum, Tacazyl, Methdilazinum [inn-latin], Metodilazina [inn-spanish]

Cas Number

1982-37-2

Unique Ingredient Identifier (UNII)

4Q13LY9Z8X

About Methdilazine

Methdilazine is a phenothiazine compound with antihistaminic activity. It is used in the treatment of various dermatoses to relieve pruritus.

Methdilazine Manufacturers

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

Methdilazine Suppliers

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

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

Methdilazine USDMF

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

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

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

Methdilazine GMP

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

Methdilazine CoA

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

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

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