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JP
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FDA Orange Book
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Data Compilation #PharmaFlow
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Listed Suppliers
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
About the Company : ChemWerth, established in 1982, is a US-headquartered full-service generic API company. It supplies cGMP-quality APIs to regulated markets worldwide, with exclusive partnerships fo...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Rochem, established in 1994, is a global distributor of pharmaceutical, food, nutritional, and animal health ingredients, sourcing high-quality products from China. Headquartered i...
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Kirsch Pharma
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High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Brand Name : Citric Acid Monohydrate
Application : Parenteral, Thickeners and Stabilizers
Excipient Details : Used as a pH regulator and preservative in many Biological formulations and cell culture media. Also it can be used as a chelating agent.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Citric Acid Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Brand Name : Trisodium Citrate
Application : Parenteral
Excipient Details : Used as a buffering agent in purification process during downstream and in the final formulation.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Trisodium Citrate Excipient
Thickeners and Stabilizers
Taste Masking
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ABOUT THIS PAGE
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PharmaCompass offers a list of Cefovecin 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 Cefovecin manufacturer or Cefovecin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefovecin manufacturer or Cefovecin supplier.
PharmaCompass also assists you with knowing the Cefovecin API Price utilized in the formulation of products. Cefovecin API Price is not always fixed or binding as the Cefovecin Price is obtained through a variety of data sources. The Cefovecin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefovecin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefovecin, including repackagers and relabelers. The FDA regulates Cefovecin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefovecin 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 Cefovecin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefovecin supplier is an individual or a company that provides Cefovecin active pharmaceutical ingredient (API) or Cefovecin finished formulations upon request. The Cefovecin suppliers may include Cefovecin API manufacturers, exporters, distributors and traders.
click here to find a list of Cefovecin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Cefovecin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cefovecin 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 Cefovecin 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 Cefovecin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cefovecin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cefovecin suppliers with NDC on PharmaCompass.
Cefovecin 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 Cefovecin 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 Cefovecin GMP manufacturer or Cefovecin GMP API supplier for your needs.
A Cefovecin CoA (Certificate of Analysis) is a formal document that attests to Cefovecin's compliance with Cefovecin specifications and serves as a tool for batch-level quality control.
Cefovecin CoA mostly includes findings from lab analyses of a specific batch. For each Cefovecin 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.
Cefovecin may be tested according to a variety of international standards, such as European Pharmacopoeia (Cefovecin EP), Cefovecin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cefovecin USP).
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