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Looking for 60282-87-3 / Gestodene API manufacturers, exporters & distributors?

Gestodene manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Gestodene

Synonyms

60282-87-3, Gestoden, Gestodenum [inn-latin], Gestodeno [inn-spanish], Sh b 331, Sh-b-331

Cas Number

60282-87-3

Unique Ingredient Identifier (UNII)

1664P6E6MI

About Gestodene

Gestodene is a progestogen hormonal contraceptive. Products containing gestoden include Meliane, which contains 20 mcg of ethinylestradiol and 75 mcg of gestodene; and Gynera, which contains 30 mcg of ethinylestradiol and 75 mcg of gestodene.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE Manufacturers

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE, including repackagers and relabelers. The FDA regulates 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE Suppliers

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE supplier is an individual or a company that provides 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE active pharmaceutical ingredient (API) or 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE finished formulations upon request. The 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE suppliers may include 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE API manufacturers, exporters, distributors and traders.

click here to find a list of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE USDMF

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE DMF (Drug Master File) is a document detailing the whole manufacturing process of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE active pharmaceutical ingredient (API) in detail. Different forms of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE DMFs exist exist since differing nations have different regulations, such as 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE DMF submitted to regulatory agencies in the US is known as a USDMF. 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE USDMF includes data on 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE suppliers with USDMF on PharmaCompass.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP of the European Pharmacopoeia monograph is often referred to as a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE Certificate of Suitability (COS). The purpose of a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE to their clients by showing that a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP has been issued for it. The manufacturer submits a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP (COS) as part of the market authorization procedure, and it takes on the role of a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP holder for the record. Additionally, the data presented in the 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE DMF.

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE suppliers with CEP (COS) on PharmaCompass.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE suppliers with NDC on PharmaCompass.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE GMP

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE GMP manufacturer or 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE GMP API supplier for your needs.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CoA

A 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CoA (Certificate of Analysis) is a formal document that attests to 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE's compliance with 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE specifications and serves as a tool for batch-level quality control.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE CoA mostly includes findings from lab analyses of a specific batch. For each 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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.

13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE may be tested according to a variety of international standards, such as European Pharmacopoeia (13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE EP), 13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (13-ETHYL-17-HYDROXY-18,19-DINOR-17.ALPHA.-PREGNA-4,15-DIEN-20-YN-3-ONE 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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