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PharmaCompass offers a list of Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride manufacturer or Acetyl-L-Carnitine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acetyl-L-Carnitine Hydrochloride manufacturer or Acetyl-L-Carnitine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Acetyl-L-Carnitine Hydrochloride API Price utilized in the formulation of products. Acetyl-L-Carnitine Hydrochloride API Price is not always fixed or binding as the Acetyl-L-Carnitine Hydrochloride Price is obtained through a variety of data sources. The Acetyl-L-Carnitine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acetyl-L-Carnitine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetyl-L-Carnitine Hydrochloride, including repackagers and relabelers. The FDA regulates Acetyl-L-Carnitine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetyl-L-Carnitine Hydrochloride supplier is an individual or a company that provides Acetyl-L-Carnitine Hydrochloride active pharmaceutical ingredient (API) or Acetyl-L-Carnitine Hydrochloride finished formulations upon request. The Acetyl-L-Carnitine Hydrochloride suppliers may include Acetyl-L-Carnitine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Acetyl-L-Carnitine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Acetyl-L-Carnitine Hydrochloride Drug Master File in Korea (Acetyl-L-Carnitine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Acetyl-L-Carnitine Hydrochloride. The MFDS reviews the Acetyl-L-Carnitine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Acetyl-L-Carnitine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Acetyl-L-Carnitine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Acetyl-L-Carnitine Hydrochloride suppliers with NDC on PharmaCompass.
Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride 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 Acetyl-L-Carnitine Hydrochloride GMP manufacturer or Acetyl-L-Carnitine Hydrochloride GMP API supplier for your needs.
A Acetyl-L-Carnitine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Acetyl-L-Carnitine Hydrochloride's compliance with Acetyl-L-Carnitine Hydrochloride specifications and serves as a tool for batch-level quality control.
Acetyl-L-Carnitine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Acetyl-L-Carnitine Hydrochloride 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.
Acetyl-L-Carnitine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Acetyl-L-Carnitine Hydrochloride EP), Acetyl-L-Carnitine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Acetyl-L-Carnitine Hydrochloride USP).