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  • SOLUTION;NASAL - 0.01%
  • SPRAY, METERED;NASAL - 0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • INJECTABLE;INJECTION - 0.004MG/ML
  • TABLET;ORAL - 0.1MG
  • TABLET;ORAL - 0.2MG
  • SPRAY, METERED;NASAL - 0.00083MG/SPRAY
  • SPRAY, METERED;NASAL - 0.00166MG/SPRAY
  • SPRAY, METERED;NASAL - 0.15MG/SPRAY
  • SPRAY, METERED;NASAL - 0.01MG/SPRAY
  • TABLET;SUBLINGUAL - 0.0277MG
  • TABLET;SUBLINGUAL - 0.0553MG

Looking for 62288-83-9 / Desmopressin Acetate API manufacturers, exporters & distributors?

Desmopressin Acetate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Desmopressin Acetate

Synonyms

Octostim, Minirin, Ddavp, Stimate, Concentraid, Desmopressin acetate anhydrous

Cas Number

62288-83-9

Unique Ingredient Identifier (UNII)

1K12647SFC

About Desmopressin Acetate

A synthetic analog of the pituitary hormone, ARGININE VASOPRESSIN. Its action is mediated by the VASOPRESSIN receptor V2. It has prolonged antidiuretic activity, but little pressor effects. It also modulates levels of circulating FACTOR VIII and VON WILLEBRAND FACTOR.

Desmopressin Acetate Manufacturers

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

Desmopressin Acetate Suppliers

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

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

Desmopressin Acetate USDMF

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

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

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

Desmopressin Acetate 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 Desmopressin Acetate Drug Master File in Japan (Desmopressin Acetate JDMF) empowers Desmopressin Acetate 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 Desmopressin Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Desmopressin Acetate 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 Desmopressin Acetate suppliers with JDMF on PharmaCompass.

Desmopressin Acetate KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Desmopressin Acetate Drug Master File in Korea (Desmopressin Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Desmopressin Acetate. The MFDS reviews the Desmopressin Acetate KDMF as part of the drug registration process and uses the information provided in the Desmopressin Acetate KDMF to evaluate the safety and efficacy of the drug.

After submitting a Desmopressin Acetate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Desmopressin Acetate API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Desmopressin Acetate suppliers with KDMF on PharmaCompass.

Desmopressin Acetate CEP

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

A Desmopressin Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desmopressin 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 Desmopressin Acetate suppliers with CEP (COS) on PharmaCompass.

Desmopressin Acetate WC

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

click here to find a list of Desmopressin Acetate suppliers with Written Confirmation (WC) on PharmaCompass.

Desmopressin 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 Desmopressin Acetate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Desmopressin 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 Desmopressin 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 Desmopressin Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Desmopressin Acetate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Desmopressin Acetate suppliers with NDC on PharmaCompass.

Desmopressin Acetate GMP

Desmopressin 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 Desmopressin 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 Desmopressin Acetate GMP manufacturer or Desmopressin Acetate GMP API supplier for your needs.

Desmopressin Acetate CoA

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

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

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