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API SUPPLIERS
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NDC API
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Pfanstiehl
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Coating Systems & Additives
Co-Processed Excipients
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Controlled & Modified Release
Granulation
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Taste Masking
Solubilizers
Topical
Film Formers & Plasticizers
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Ammonium Carbonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ammonium Carbonate, including repackagers and relabelers. The FDA regulates Ammonium Carbonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ammonium Carbonate 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 Ammonium Carbonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ammonium Carbonate supplier is an individual or a company that provides Ammonium Carbonate active pharmaceutical ingredient (API) or Ammonium Carbonate finished formulations upon request. The Ammonium Carbonate suppliers may include Ammonium Carbonate API manufacturers, exporters, distributors and traders.
click here to find a list of Ammonium Carbonate 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 Ammonium Carbonate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ammonium Carbonate 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 Ammonium Carbonate 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 Ammonium Carbonate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ammonium Carbonate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ammonium Carbonate suppliers with NDC on PharmaCompass.
Ammonium Carbonate 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 Ammonium Carbonate 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 Ammonium Carbonate GMP manufacturer or Ammonium Carbonate GMP API supplier for your needs.
A Ammonium Carbonate CoA (Certificate of Analysis) is a formal document that attests to Ammonium Carbonate's compliance with Ammonium Carbonate specifications and serves as a tool for batch-level quality control.
Ammonium Carbonate CoA mostly includes findings from lab analyses of a specific batch. For each Ammonium Carbonate 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.
Ammonium Carbonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ammonium Carbonate EP), Ammonium Carbonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ammonium Carbonate USP).
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