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PharmaCompass offers a list of Dl-Methylephedrine 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 Dl-Methylephedrine Hydrochloride manufacturer or Dl-Methylephedrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dl-Methylephedrine Hydrochloride manufacturer or Dl-Methylephedrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dl-Methylephedrine Hydrochloride API Price utilized in the formulation of products. Dl-Methylephedrine Hydrochloride API Price is not always fixed or binding as the Dl-Methylephedrine Hydrochloride Price is obtained through a variety of data sources. The Dl-Methylephedrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dl-Methylephedrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dl-Methylephedrine Hydrochloride, including repackagers and relabelers. The FDA regulates Dl-Methylephedrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dl-Methylephedrine 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.
A Dl-Methylephedrine Hydrochloride supplier is an individual or a company that provides Dl-Methylephedrine Hydrochloride active pharmaceutical ingredient (API) or Dl-Methylephedrine Hydrochloride finished formulations upon request. The Dl-Methylephedrine Hydrochloride suppliers may include Dl-Methylephedrine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dl-Methylephedrine 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 Dl-Methylephedrine Hydrochloride Drug Master File in Korea (Dl-Methylephedrine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dl-Methylephedrine Hydrochloride. The MFDS reviews the Dl-Methylephedrine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Dl-Methylephedrine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dl-Methylephedrine 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 Dl-Methylephedrine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dl-Methylephedrine Hydrochloride suppliers with KDMF on PharmaCompass.
A Dl-Methylephedrine Hydrochloride written confirmation (Dl-Methylephedrine Hydrochloride WC) is an official document issued by a regulatory agency to a Dl-Methylephedrine Hydrochloride manufacturer, verifying that the manufacturing facility of a Dl-Methylephedrine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dl-Methylephedrine Hydrochloride APIs or Dl-Methylephedrine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Dl-Methylephedrine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Dl-Methylephedrine Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
Dl-Methylephedrine 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 Dl-Methylephedrine 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 Dl-Methylephedrine Hydrochloride GMP manufacturer or Dl-Methylephedrine Hydrochloride GMP API supplier for your needs.
A Dl-Methylephedrine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Dl-Methylephedrine Hydrochloride's compliance with Dl-Methylephedrine Hydrochloride specifications and serves as a tool for batch-level quality control.
Dl-Methylephedrine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Dl-Methylephedrine 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.
Dl-Methylephedrine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Dl-Methylephedrine Hydrochloride EP), Dl-Methylephedrine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dl-Methylephedrine Hydrochloride USP).
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