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PharmaCompass offers a list of Ammonia 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 Ammonia manufacturer or Ammonia supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ammonia manufacturer or Ammonia supplier.
PharmaCompass also assists you with knowing the Ammonia API Price utilized in the formulation of products. Ammonia API Price is not always fixed or binding as the Ammonia Price is obtained through a variety of data sources. The Ammonia Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (13n)ammonia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (13n)ammonia, including repackagers and relabelers. The FDA regulates (13n)ammonia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (13n)ammonia 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 (13n)ammonia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (13n)ammonia supplier is an individual or a company that provides (13n)ammonia active pharmaceutical ingredient (API) or (13n)ammonia finished formulations upon request. The (13n)ammonia suppliers may include (13n)ammonia API manufacturers, exporters, distributors and traders.
click here to find a list of (13n)ammonia suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
(13n)ammonia 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 (13n)ammonia 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 (13n)ammonia GMP manufacturer or (13n)ammonia GMP API supplier for your needs.
A (13n)ammonia CoA (Certificate of Analysis) is a formal document that attests to (13n)ammonia's compliance with (13n)ammonia specifications and serves as a tool for batch-level quality control.
(13n)ammonia CoA mostly includes findings from lab analyses of a specific batch. For each (13n)ammonia 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.
(13n)ammonia may be tested according to a variety of international standards, such as European Pharmacopoeia ((13n)ammonia EP), (13n)ammonia JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((13n)ammonia USP).