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ABOUT THIS PAGE
A Pentetic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentetic Acid, including repackagers and relabelers. The FDA regulates Pentetic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentetic Acid 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 Pentetic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pentetic Acid supplier is an individual or a company that provides Pentetic Acid active pharmaceutical ingredient (API) or Pentetic Acid finished formulations upon request. The Pentetic Acid suppliers may include Pentetic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Pentetic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pentetic Acid DMF (Drug Master File) is a document detailing the whole manufacturing process of Pentetic Acid active pharmaceutical ingredient (API) in detail. Different forms of Pentetic Acid DMFs exist exist since differing nations have different regulations, such as Pentetic Acid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pentetic Acid DMF submitted to regulatory agencies in the US is known as a USDMF. Pentetic Acid USDMF includes data on Pentetic Acid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pentetic Acid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pentetic Acid suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Pentetic Acid Drug Master File in Korea (Pentetic Acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pentetic Acid. The MFDS reviews the Pentetic Acid KDMF as part of the drug registration process and uses the information provided in the Pentetic Acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pentetic Acid KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Pentetic Acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pentetic Acid suppliers with KDMF 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 Pentetic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pentetic Acid 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 Pentetic Acid 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 Pentetic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pentetic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pentetic Acid suppliers with NDC on PharmaCompass.
Pentetic Acid 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 Pentetic Acid 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 Pentetic Acid GMP manufacturer or Pentetic Acid GMP API supplier for your needs.
A Pentetic Acid CoA (Certificate of Analysis) is a formal document that attests to Pentetic Acid's compliance with Pentetic Acid specifications and serves as a tool for batch-level quality control.
Pentetic Acid CoA mostly includes findings from lab analyses of a specific batch. For each Pentetic Acid 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.
Pentetic Acid may be tested according to a variety of international standards, such as European Pharmacopoeia (Pentetic Acid EP), Pentetic Acid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pentetic Acid USP).
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