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Looking for 920014-72-8 / Setmelanotide Acetate API manufacturers, exporters & distributors?

Setmelanotide Acetate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Setmelanotide Acetate

Synonyms

920014-72-8, Rm-493, Bim-22493, N7t15v1fuy, (4r,7s,10s,13r,16s,19r,22r)-22-[[(2s)-2-acetamido-5-(diaminomethylideneamino)pentanoyl]amino]-13-benzyl-10-[3-(diaminomethylideneamino)propyl]-16-(1h-imidazol-5-ylmethyl)-7-(1h-indol-3-ylmethyl)-19-methyl-6,9,12,15,18,21-hexaoxo-1,2-dithia-5,8,11,14,17,20-hexazacyclotricosane-4-carboxamide, 1504602-49-6

Cas Number

920014-72-8

Unique Ingredient Identifier (UNII)

N7T15V1FUY

About Setmelanotide Acetate

Setmelanotide is the first available treatment for patients with pro-opiomelanocortin, proprotein subilisin/kexin type 1, or leptin deficiencies. It is an agonist of the melanocortin 4 receptor. Earlier attempts at agonizing MC4R (such as LY2112688) lead to successful weight loss, but also an increase in blood pressure and heart rate. Other earlier treatments for these patients included gastric bypass surgery. Patients taking setmelanotide experienced an average weight loss of 0.6 kg/week. Imcivree was granted EMA orphan designation on 19 November 2018 and FDA approval on 25 November 2020.

Setmelanotide Acetate Manufacturers

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

Setmelanotide Acetate Suppliers

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

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

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

Finished drug products

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

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

Setmelanotide Acetate GMP

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

Setmelanotide Acetate CoA

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

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

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