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Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
About the Company : Malladi Drugs & Pharmaceuticals Ltd, founded in 1980 by Mr. M L N Sastry, is a leader in manufacturing ephedrine and pseudoephedrine salts. It is now the top API manufacturer in th...
Anlon Healthcare manufactures high-quality Pharmaceutical Bulk Drugs & Intermediates compliant with FDA, PMDA, KFDA, cGMP & WHO-GMP.
About the Company : Anlon Healthcare is a research-focused pharmaceutical manufacturer based in Rajkot, specializing in bulk drugs and intermediates. The company’s products comply with international...
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
About the Company : Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It specializes in researching, developing and producing active pharmaceutical ingr...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
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02 Oct 2018
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REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Butamirate Citrate 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 Butamirate Citrate manufacturer or Butamirate Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Butamirate Citrate manufacturer or Butamirate Citrate supplier.
PharmaCompass also assists you with knowing the Butamirate Citrate API Price utilized in the formulation of products. Butamirate Citrate API Price is not always fixed or binding as the Butamirate Citrate Price is obtained through a variety of data sources. The Butamirate Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Butamirate Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butamirate Citrate, including repackagers and relabelers. The FDA regulates Butamirate Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butamirate Citrate 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 Butamirate Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Butamirate Citrate supplier is an individual or a company that provides Butamirate Citrate active pharmaceutical ingredient (API) or Butamirate Citrate finished formulations upon request. The Butamirate Citrate suppliers may include Butamirate Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Butamirate Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Butamirate Citrate written confirmation (Butamirate Citrate WC) is an official document issued by a regulatory agency to a Butamirate Citrate manufacturer, verifying that the manufacturing facility of a Butamirate Citrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Butamirate Citrate APIs or Butamirate Citrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Butamirate Citrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Butamirate Citrate suppliers with Written Confirmation (WC) on PharmaCompass.
Butamirate Citrate 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 Butamirate Citrate 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 Butamirate Citrate GMP manufacturer or Butamirate Citrate GMP API supplier for your needs.
A Butamirate Citrate CoA (Certificate of Analysis) is a formal document that attests to Butamirate Citrate's compliance with Butamirate Citrate specifications and serves as a tool for batch-level quality control.
Butamirate Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Butamirate Citrate 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.
Butamirate Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Butamirate Citrate EP), Butamirate Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Butamirate Citrate USP).
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