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USDMF
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DOSAGE - INJECTABLE;INTRAVENOUS - 20MG/200ML ...DOSAGE - INJECTABLE;INTRAVENOUS - 20MG/200ML (0.1MG/ML)
USFDA APPLICATION NUMBER - 19734
DOSAGE - INJECTABLE;INJECTION - 25MG/10ML (2....DOSAGE - INJECTABLE;INJECTION - 25MG/10ML (2.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 19734
DOSAGE - INJECTABLE;INTRAVENOUS - 40MG/200ML ...DOSAGE - INJECTABLE;INTRAVENOUS - 40MG/200ML (0.2MG/ML)
USFDA APPLICATION NUMBER - 19734
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ABOUT THIS PAGE
A Perdipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perdipine, including repackagers and relabelers. The FDA regulates Perdipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perdipine 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 Perdipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Perdipine supplier is an individual or a company that provides Perdipine active pharmaceutical ingredient (API) or Perdipine finished formulations upon request. The Perdipine suppliers may include Perdipine API manufacturers, exporters, distributors and traders.
click here to find a list of Perdipine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Perdipine DMF (Drug Master File) is a document detailing the whole manufacturing process of Perdipine active pharmaceutical ingredient (API) in detail. Different forms of Perdipine DMFs exist exist since differing nations have different regulations, such as Perdipine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Perdipine DMF submitted to regulatory agencies in the US is known as a USDMF. Perdipine USDMF includes data on Perdipine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Perdipine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Perdipine 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 Perdipine Drug Master File in Japan (Perdipine JDMF) empowers Perdipine 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 Perdipine JDMF during the approval evaluation for pharmaceutical products. At the time of Perdipine 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 Perdipine 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 Perdipine Drug Master File in Korea (Perdipine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Perdipine. The MFDS reviews the Perdipine KDMF as part of the drug registration process and uses the information provided in the Perdipine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Perdipine 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 Perdipine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Perdipine suppliers with KDMF on PharmaCompass.
A Perdipine written confirmation (Perdipine WC) is an official document issued by a regulatory agency to a Perdipine manufacturer, verifying that the manufacturing facility of a Perdipine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Perdipine APIs or Perdipine finished pharmaceutical products to another nation, regulatory agencies frequently require a Perdipine WC (written confirmation) as part of the regulatory process.
click here to find a list of Perdipine 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 Perdipine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Perdipine 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 Perdipine 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 Perdipine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Perdipine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Perdipine suppliers with NDC on PharmaCompass.
Perdipine 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 Perdipine 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 Perdipine GMP manufacturer or Perdipine GMP API supplier for your needs.
A Perdipine CoA (Certificate of Analysis) is a formal document that attests to Perdipine's compliance with Perdipine specifications and serves as a tool for batch-level quality control.
Perdipine CoA mostly includes findings from lab analyses of a specific batch. For each Perdipine 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.
Perdipine may be tested according to a variety of international standards, such as European Pharmacopoeia (Perdipine EP), Perdipine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Perdipine USP).
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