Synopsis
0
USDMF
0
JDMF
0
EU WC
0
KDMF
0
FDF
0
FDA Orange Book
0
Europe
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Digital Content
NEWS #PharmaBuzz
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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.
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.
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.
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).
The FDA updates the NDC directory daily. The NDC numbers for Selamectin API and other APIs are published in this directory by the FDA.
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.
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 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.
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).
LOOKING FOR A SUPPLIER?
