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PharmaCompass offers a list of Propranolol 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 Propranolol Hydrochloride manufacturer or Propranolol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propranolol Hydrochloride manufacturer or Propranolol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Propranolol Hydrochloride API Price utilized in the formulation of products. Propranolol Hydrochloride API Price is not always fixed or binding as the Propranolol Hydrochloride Price is obtained through a variety of data sources. The Propranolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Propranolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propranolol Hydrochloride, including repackagers and relabelers. The FDA regulates Propranolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propranolol 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 Propranolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propranolol Hydrochloride supplier is an individual or a company that provides Propranolol Hydrochloride active pharmaceutical ingredient (API) or Propranolol Hydrochloride finished formulations upon request. The Propranolol Hydrochloride suppliers may include Propranolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Propranolol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Propranolol Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Propranolol Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Propranolol Hydrochloride DMFs exist exist since differing nations have different regulations, such as Propranolol Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Propranolol Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Propranolol Hydrochloride USDMF includes data on Propranolol Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Propranolol Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Propranolol Hydrochloride suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Propranolol Hydrochloride Drug Master File in Japan (Propranolol Hydrochloride JDMF) empowers Propranolol Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Propranolol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Propranolol Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Propranolol Hydrochloride suppliers with JDMF on PharmaCompass.
A Propranolol Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Propranolol Hydrochloride Certificate of Suitability (COS). The purpose of a Propranolol Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Propranolol Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Propranolol Hydrochloride to their clients by showing that a Propranolol Hydrochloride CEP has been issued for it. The manufacturer submits a Propranolol Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Propranolol Hydrochloride CEP holder for the record. Additionally, the data presented in the Propranolol Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Propranolol Hydrochloride DMF.
A Propranolol Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Propranolol Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Propranolol Hydrochloride suppliers with CEP (COS) on PharmaCompass.
A Propranolol Hydrochloride written confirmation (Propranolol Hydrochloride WC) is an official document issued by a regulatory agency to a Propranolol Hydrochloride manufacturer, verifying that the manufacturing facility of a Propranolol Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Propranolol Hydrochloride APIs or Propranolol Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Propranolol Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Propranolol 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 Propranolol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Propranolol 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 Propranolol 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 Propranolol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Propranolol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Propranolol Hydrochloride suppliers with NDC on PharmaCompass.
Propranolol 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 Propranolol 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 Propranolol Hydrochloride GMP manufacturer or Propranolol Hydrochloride GMP API supplier for your needs.
A Propranolol Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Propranolol Hydrochloride's compliance with Propranolol Hydrochloride specifications and serves as a tool for batch-level quality control.
Propranolol Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Propranolol 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.
Propranolol Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Propranolol Hydrochloride EP), Propranolol Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Propranolol Hydrochloride USP).