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Looking for 220119-17-5 / Selamectin API manufacturers, exporters & distributors?

Selamectin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Selamectin

Synonyms

Revolution, 220119-17-5, Uk-124,114, 165108-07-6, Uk-124114, A2669owx9n

Cas Number

220119-17-5

Unique Ingredient Identifier (UNII)

A2669OWX9N

About Selamectin

Selamectin is a topical parasiticide and antihelminthic used on dogs and cats to treat and prevent infections of heartworms, fleas, ear mites, sarcoptic mange, and certain types of ticks in dogs as well as prevent heartworms, fleas, ear mites, hookworms, and roundworms in cats. It also removes 2 types of lungworm in cats and one type of lungworm in dogs. It is distributed by Zoetis, a former Pfizer subsidiary. It is structurally related to ivermectin and milbemycin. Selamectin is not approved for human use.

Selamectin Manufacturers

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

Selamectin Suppliers

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

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

Selamectin CEP

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

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

Selamectin 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 Selamectin as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Selamectin GMP

Selamectin 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 Selamectin 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 Selamectin GMP manufacturer or Selamectin GMP API supplier for your needs.

Selamectin CoA

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

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

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