X
API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
USA (Orange Book)
Europe
0
Canada
0
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
43
PharmaCompass offers a list of gamma-BHC 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 gamma-BHC manufacturer or gamma-BHC supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred gamma-BHC manufacturer or gamma-BHC supplier.
PharmaCompass also assists you with knowing the gamma-BHC API Price utilized in the formulation of products. gamma-BHC API Price is not always fixed or binding as the gamma-BHC Price is obtained through a variety of data sources. The gamma-BHC Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lindane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lindane, including repackagers and relabelers. The FDA regulates Lindane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lindane API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Lindane supplier is an individual or a company that provides Lindane active pharmaceutical ingredient (API) or Lindane finished formulations upon request. The Lindane suppliers may include Lindane API manufacturers, exporters, distributors and traders.
click here to find a list of Lindane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lindane DMF (Drug Master File) is a document detailing the whole manufacturing process of Lindane active pharmaceutical ingredient (API) in detail. Different forms of Lindane DMFs exist exist since differing nations have different regulations, such as Lindane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lindane DMF submitted to regulatory agencies in the US is known as a USDMF. Lindane USDMF includes data on Lindane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lindane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lindane suppliers with USDMF on PharmaCompass.
A Lindane CEP of the European Pharmacopoeia monograph is often referred to as a Lindane Certificate of Suitability (COS). The purpose of a Lindane CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lindane EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lindane to their clients by showing that a Lindane CEP has been issued for it. The manufacturer submits a Lindane CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lindane CEP holder for the record. Additionally, the data presented in the Lindane CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lindane DMF.
A Lindane CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lindane 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 Lindane suppliers with CEP (COS) on PharmaCompass.
Lindane 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 Lindane 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 Lindane GMP manufacturer or Lindane GMP API supplier for your needs.
A Lindane CoA (Certificate of Analysis) is a formal document that attests to Lindane's compliance with Lindane specifications and serves as a tool for batch-level quality control.
Lindane CoA mostly includes findings from lab analyses of a specific batch. For each Lindane 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.
Lindane may be tested according to a variety of international standards, such as European Pharmacopoeia (Lindane EP), Lindane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lindane USP).
Market Place
