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Looking for 58652-20-3 / Nomegestrol Acetate API manufacturers, exporters & distributors?

Nomegestrol Acetate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Nomegestrol Acetate

Synonyms

58652-20-3, Nomegestrol 17-acetate, Tx 066, Tx-066, 19-norpregna-4,6-diene-3,20-dione, 17-(acetyloxy)-6-methyl-, Nomegestrol acetate [usan]

Cas Number

58652-20-3

Unique Ingredient Identifier (UNII)

83J78V5W05

About Nomegestrol Acetate

Nomegestrol acetate, also known as NOMAC, is a progestin used in oral contraceptives, menopausal hormone therapy, and for the treatment of gynecological disorders.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate Manufacturers

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate, including repackagers and relabelers. The FDA regulates 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate 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-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate Suppliers

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate supplier is an individual or a company that provides 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate active pharmaceutical ingredient (API) or 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate finished formulations upon request. The 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate suppliers may include 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate API manufacturers, exporters, distributors and traders.

click here to find a list of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate USDMF

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate DMF (Drug Master File) is a document detailing the whole manufacturing process of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate active pharmaceutical ingredient (API) in detail. Different forms of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate DMFs exist exist since differing nations have different regulations, such as 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate DMF submitted to regulatory agencies in the US is known as a USDMF. 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate USDMF includes data on 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate suppliers with USDMF on PharmaCompass.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP of the European Pharmacopoeia monograph is often referred to as a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate Certificate of Suitability (COS). The purpose of a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate to their clients by showing that a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP has been issued for it. The manufacturer submits a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP holder for the record. Additionally, the data presented in the 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate DMF.

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate suppliers with CEP (COS) on PharmaCompass.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate suppliers with NDC on PharmaCompass.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate GMP

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate 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-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate 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-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate GMP manufacturer or 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate GMP API supplier for your needs.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CoA

A 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CoA (Certificate of Analysis) is a formal document that attests to 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate's compliance with 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate specifications and serves as a tool for batch-level quality control.

17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate CoA mostly includes findings from lab analyses of a specific batch. For each 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate 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-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate EP), 17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (17-alpha-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate 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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