X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
Other Suppliers
0
USA (Orange Book)
Europe
Canada
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
14
PharmaCompass offers a list of Phenylpropanolamine 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 Phenylpropanolamine manufacturer or Phenylpropanolamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylpropanolamine manufacturer or Phenylpropanolamine supplier.
PharmaCompass also assists you with knowing the Phenylpropanolamine API Price utilized in the formulation of products. Phenylpropanolamine API Price is not always fixed or binding as the Phenylpropanolamine Price is obtained through a variety of data sources. The Phenylpropanolamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dl-Norephedrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dl-Norephedrine Hydrochloride, including repackagers and relabelers. The FDA regulates Dl-Norephedrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dl-Norephedrine 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 Dl-Norephedrine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dl-Norephedrine Hydrochloride supplier is an individual or a company that provides Dl-Norephedrine Hydrochloride active pharmaceutical ingredient (API) or Dl-Norephedrine Hydrochloride finished formulations upon request. The Dl-Norephedrine Hydrochloride suppliers may include Dl-Norephedrine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dl-Norephedrine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dl-Norephedrine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Dl-Norephedrine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Dl-Norephedrine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Dl-Norephedrine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dl-Norephedrine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Dl-Norephedrine Hydrochloride USDMF includes data on Dl-Norephedrine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dl-Norephedrine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dl-Norephedrine Hydrochloride suppliers with USDMF on PharmaCompass.
A Dl-Norephedrine Hydrochloride written confirmation (Dl-Norephedrine Hydrochloride WC) is an official document issued by a regulatory agency to a Dl-Norephedrine Hydrochloride manufacturer, verifying that the manufacturing facility of a Dl-Norephedrine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dl-Norephedrine Hydrochloride APIs or Dl-Norephedrine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Dl-Norephedrine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Dl-Norephedrine Hydrochloride suppliers with Written Confirmation (WC) 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 Dl-Norephedrine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dl-Norephedrine 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 Dl-Norephedrine 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 Dl-Norephedrine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dl-Norephedrine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dl-Norephedrine Hydrochloride suppliers with NDC on PharmaCompass.
Dl-Norephedrine 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-Norephedrine 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-Norephedrine Hydrochloride GMP manufacturer or Dl-Norephedrine Hydrochloride GMP API supplier for your needs.
A Dl-Norephedrine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Dl-Norephedrine Hydrochloride's compliance with Dl-Norephedrine Hydrochloride specifications and serves as a tool for batch-level quality control.
Dl-Norephedrine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Dl-Norephedrine 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-Norephedrine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Dl-Norephedrine Hydrochloride EP), Dl-Norephedrine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dl-Norephedrine Hydrochloride USP).
Market Place
