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Looking for 432-60-0 / Allylestrenol API manufacturers, exporters & distributors?

Allylestrenol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Allylestrenol

Synonyms

432-60-0, Gestanin, Gestanon, Allyloestrenol, Gestanol, Orageston

Cas Number

432-60-0

Unique Ingredient Identifier (UNII)

I47VB5DZ8O

About Allylestrenol

A synthetic steroid with progestational activity.

17-alpha-Allyl-4-oestrene-17-beta-ol Manufacturers

A 17-alpha-Allyl-4-oestrene-17-beta-ol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 17-alpha-Allyl-4-oestrene-17-beta-ol, including repackagers and relabelers. The FDA regulates 17-alpha-Allyl-4-oestrene-17-beta-ol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 17-alpha-Allyl-4-oestrene-17-beta-ol 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 17-alpha-Allyl-4-oestrene-17-beta-ol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

17-alpha-Allyl-4-oestrene-17-beta-ol Suppliers

A 17-alpha-Allyl-4-oestrene-17-beta-ol supplier is an individual or a company that provides 17-alpha-Allyl-4-oestrene-17-beta-ol active pharmaceutical ingredient (API) or 17-alpha-Allyl-4-oestrene-17-beta-ol finished formulations upon request. The 17-alpha-Allyl-4-oestrene-17-beta-ol suppliers may include 17-alpha-Allyl-4-oestrene-17-beta-ol API manufacturers, exporters, distributors and traders.

click here to find a list of 17-alpha-Allyl-4-oestrene-17-beta-ol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

17-alpha-Allyl-4-oestrene-17-beta-ol JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The 17-alpha-Allyl-4-oestrene-17-beta-ol Drug Master File in Japan (17-alpha-Allyl-4-oestrene-17-beta-ol JDMF) empowers 17-alpha-Allyl-4-oestrene-17-beta-ol API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the 17-alpha-Allyl-4-oestrene-17-beta-ol JDMF during the approval evaluation for pharmaceutical products. At the time of 17-alpha-Allyl-4-oestrene-17-beta-ol JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of 17-alpha-Allyl-4-oestrene-17-beta-ol suppliers with JDMF on PharmaCompass.

17-alpha-Allyl-4-oestrene-17-beta-ol WC

A 17-alpha-Allyl-4-oestrene-17-beta-ol written confirmation (17-alpha-Allyl-4-oestrene-17-beta-ol WC) is an official document issued by a regulatory agency to a 17-alpha-Allyl-4-oestrene-17-beta-ol manufacturer, verifying that the manufacturing facility of a 17-alpha-Allyl-4-oestrene-17-beta-ol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 17-alpha-Allyl-4-oestrene-17-beta-ol APIs or 17-alpha-Allyl-4-oestrene-17-beta-ol finished pharmaceutical products to another nation, regulatory agencies frequently require a 17-alpha-Allyl-4-oestrene-17-beta-ol WC (written confirmation) as part of the regulatory process.

click here to find a list of 17-alpha-Allyl-4-oestrene-17-beta-ol suppliers with Written Confirmation (WC) on PharmaCompass.

17-alpha-Allyl-4-oestrene-17-beta-ol GMP

17-alpha-Allyl-4-oestrene-17-beta-ol 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 17-alpha-Allyl-4-oestrene-17-beta-ol 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 17-alpha-Allyl-4-oestrene-17-beta-ol GMP manufacturer or 17-alpha-Allyl-4-oestrene-17-beta-ol GMP API supplier for your needs.

17-alpha-Allyl-4-oestrene-17-beta-ol CoA

A 17-alpha-Allyl-4-oestrene-17-beta-ol CoA (Certificate of Analysis) is a formal document that attests to 17-alpha-Allyl-4-oestrene-17-beta-ol's compliance with 17-alpha-Allyl-4-oestrene-17-beta-ol specifications and serves as a tool for batch-level quality control.

17-alpha-Allyl-4-oestrene-17-beta-ol CoA mostly includes findings from lab analyses of a specific batch. For each 17-alpha-Allyl-4-oestrene-17-beta-ol 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.

17-alpha-Allyl-4-oestrene-17-beta-ol may be tested according to a variety of international standards, such as European Pharmacopoeia (17-alpha-Allyl-4-oestrene-17-beta-ol EP), 17-alpha-Allyl-4-oestrene-17-beta-ol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (17-alpha-Allyl-4-oestrene-17-beta-ol 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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