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API SUPPLIERS
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USDMF
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DOSAGE - TABLET, ORALLY DISINTEGRATING;ORAL -...DOSAGE - TABLET, ORALLY DISINTEGRATING;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 200179
DOSAGE - TABLET;ORAL - EQ 10MG BASE **Federal...DOSAGE - TABLET;ORAL - EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21400
DOSAGE - TABLET;ORAL - EQ 2.5MG BASE **Federa...DOSAGE - TABLET;ORAL - EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21400
DOSAGE - TABLET;ORAL - EQ 20MG BASE **Federal...DOSAGE - TABLET;ORAL - EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21400
DOSAGE - TABLET;ORAL - EQ 5MG BASE **Federal ...DOSAGE - TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21400
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ABOUT THIS PAGE
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PharmaCompass offers a list of Vardenafil 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 Vardenafil Hydrochloride manufacturer or Vardenafil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vardenafil Hydrochloride manufacturer or Vardenafil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Vardenafil Hydrochloride API Price utilized in the formulation of products. Vardenafil Hydrochloride API Price is not always fixed or binding as the Vardenafil Hydrochloride Price is obtained through a variety of data sources. The Vardenafil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vardenafil HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vardenafil HCl, including repackagers and relabelers. The FDA regulates Vardenafil HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vardenafil HCl 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 Vardenafil HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vardenafil HCl supplier is an individual or a company that provides Vardenafil HCl active pharmaceutical ingredient (API) or Vardenafil HCl finished formulations upon request. The Vardenafil HCl suppliers may include Vardenafil HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Vardenafil HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vardenafil HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Vardenafil HCl active pharmaceutical ingredient (API) in detail. Different forms of Vardenafil HCl DMFs exist exist since differing nations have different regulations, such as Vardenafil HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vardenafil HCl DMF submitted to regulatory agencies in the US is known as a USDMF. Vardenafil HCl USDMF includes data on Vardenafil HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vardenafil HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vardenafil HCl 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 Vardenafil HCl Drug Master File in Japan (Vardenafil HCl JDMF) empowers Vardenafil HCl 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 Vardenafil HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Vardenafil HCl 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 Vardenafil HCl suppliers with JDMF 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 Vardenafil HCl Drug Master File in Korea (Vardenafil HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vardenafil HCl. The MFDS reviews the Vardenafil HCl KDMF as part of the drug registration process and uses the information provided in the Vardenafil HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vardenafil HCl 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 Vardenafil HCl API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vardenafil HCl suppliers with KDMF on PharmaCompass.
A Vardenafil HCl CEP of the European Pharmacopoeia monograph is often referred to as a Vardenafil HCl Certificate of Suitability (COS). The purpose of a Vardenafil HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vardenafil HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vardenafil HCl to their clients by showing that a Vardenafil HCl CEP has been issued for it. The manufacturer submits a Vardenafil HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vardenafil HCl CEP holder for the record. Additionally, the data presented in the Vardenafil HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vardenafil HCl DMF.
A Vardenafil HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vardenafil HCl 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 Vardenafil HCl suppliers with CEP (COS) on PharmaCompass.
A Vardenafil HCl written confirmation (Vardenafil HCl WC) is an official document issued by a regulatory agency to a Vardenafil HCl manufacturer, verifying that the manufacturing facility of a Vardenafil HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vardenafil HCl APIs or Vardenafil HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Vardenafil HCl WC (written confirmation) as part of the regulatory process.
click here to find a list of Vardenafil HCl 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 Vardenafil HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vardenafil HCl 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 Vardenafil HCl 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 Vardenafil HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vardenafil HCl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vardenafil HCl suppliers with NDC on PharmaCompass.
Vardenafil HCl 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 Vardenafil HCl 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 Vardenafil HCl GMP manufacturer or Vardenafil HCl GMP API supplier for your needs.
A Vardenafil HCl CoA (Certificate of Analysis) is a formal document that attests to Vardenafil HCl's compliance with Vardenafil HCl specifications and serves as a tool for batch-level quality control.
Vardenafil HCl CoA mostly includes findings from lab analyses of a specific batch. For each Vardenafil HCl 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.
Vardenafil HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Vardenafil HCl EP), Vardenafil HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vardenafil HCl USP).
