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Looking for 852626-89-2 / Samidorphan L-Malate API manufacturers, exporters & distributors?

Samidorphan L-Malate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Samidorphan L-Malate 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 Samidorphan L-Malate manufacturer or Samidorphan L-Malate supplier for your needs.

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

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

API | Excipient name

Samidorphan L-Malate

Synonyms

852626-89-2, Alks 33, Alks-33, Samidorphan [usan], Rdc-0313-00, Chembl426084

Cas Number

852626-89-2

Unique Ingredient Identifier (UNII)

7W2581Z5L8

About Samidorphan L-Malate

[Olanzapine] is an effective atypical antipsychotic that, like other antipsychotics, is associated with weight gain, metabolic dysfunction, and increased risk of type II diabetes. Samidorphan is a novel opioid antagonist structurally related to [naltrexone], with a higher affinity for opioid receptors, more potent -opioid receptor antagonism, higher oral bioavailability, and a longer half-life, making it an attractive candidate for oral dosing. Although antipsychotic-induced weight gain is incompletely understood, it is thought that the opioid system plays a key role in feeding and metabolism, such that opioid antagonism may be expected to ameliorate these negative effects. Samidorphan has been shown in animal models and clinical trials to ameliorate [olanzapine]-induced weight gain and metabolic dysfunction. Samidorphan was first approved as a variety of fixed-dose combination tablets with [olanzapine] by the FDA on May 28, 2021, and is currently marketed under the trademark LYBALVI by Alkermes Inc.

Samidorphan L-Malate Manufacturers

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

Samidorphan L-Malate Suppliers

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

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

Samidorphan L-Malate 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 Samidorphan L-Malate as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Samidorphan L-Malate suppliers with NDC on PharmaCompass.

Samidorphan L-Malate GMP

Samidorphan L-Malate 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 Samidorphan L-Malate 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 Samidorphan L-Malate GMP manufacturer or Samidorphan L-Malate GMP API supplier for your needs.

Samidorphan L-Malate CoA

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

Samidorphan L-Malate CoA mostly includes findings from lab analyses of a specific batch. For each Samidorphan L-Malate 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.

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