Synopsis
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JDMF
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VMF
DRUG PRODUCT COMPOSITIONS0
Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
Jai Radhe Sales is your partner for all your sourcing needs.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Emay Pharmaceuticals is a GMP-certified API manufacturing company.
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
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USDMF
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Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
About the Company : Zeal MediPharma is a globally recognized Star One Export House, serving customers in over 50 countries for more than two decades. We specialize in sourcing and exporting high-quali...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Emay Pharmaceuticals is a GMP-certified API manufacturing company.
About the Company : Emay Pharmaceuticals Pvt Ltd functions as the merchant export division of M/s. Bhavna Laboratories Pvt Ltd. As a GMP-approved API manufacturing company, we boast over three decades...
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
About the Company : With a history spanning over three decades, IOL Chemicals and Pharmaceuticals Limited is an innovation-driven company that specializes in bulk drugs, intermediates and specialty ch...
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Pharm-Rx has earned an outstanding reputation since its establishment in 1991, serving as a reputable importer and distributor of active ingredients to the pharmaceutical, nutritio...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
About the Company : Zeon Pharma Industries India Pvt ltd is an ISO & GMP certified manufacturer of Bulk drugs & Intermediate and also supplies our associate manufacturing plant API / Semi finish form...
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API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
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IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
2,4-Diamino-6-chloropyrimidine (2,4-DACP)
CAS Number : 156-83-2
End Use API : Minoxidil
About The Company : With a history spanning over three decades, IOL Chemicals and Pharmaceuticals Limited is an innovation-driven company that specializes in bulk drugs, intermedia...
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
2,4-Diamino-6-chloropyrimidine 3-N-Oxide
CAS Number : 35139-67-4
End Use API : Minoxidil
About The Company : With a history spanning over three decades, IOL Chemicals and Pharmaceuticals Limited is an innovation-driven company that specializes in bulk drugs, intermedia...
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DOSAGE - SOLUTION;TOPICAL - 2%
USFDA APPLICATION NUMBER - 19501
DOSAGE - SOLUTION;TOPICAL - 5%
USFDA APPLICATION NUMBER - 20834
DOSAGE - AEROSOL, FOAM;TOPICAL - 5%
USFDA APPLICATION NUMBER - 21812
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Digital Content
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US Medicaid Prescriptions
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Minoxidil 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 Minoxidil manufacturer or Minoxidil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Minoxidil manufacturer or Minoxidil supplier.
PharmaCompass also assists you with knowing the Minoxidil API Price utilized in the formulation of products. Minoxidil API Price is not always fixed or binding as the Minoxidil Price is obtained through a variety of data sources. The Minoxidil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Avacor and Mintop manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Avacor and Mintop, including repackagers and relabelers. The FDA regulates Avacor and Mintop manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Avacor and Mintop 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 Avacor and Mintop manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Avacor and Mintop supplier is an individual or a company that provides Avacor and Mintop active pharmaceutical ingredient (API) or Avacor and Mintop finished formulations upon request. The Avacor and Mintop suppliers may include Avacor and Mintop API manufacturers, exporters, distributors and traders.
click here to find a list of Avacor and Mintop suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Avacor and Mintop DMF (Drug Master File) is a document detailing the whole manufacturing process of Avacor and Mintop active pharmaceutical ingredient (API) in detail. Different forms of Avacor and Mintop DMFs exist exist since differing nations have different regulations, such as Avacor and Mintop USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Avacor and Mintop DMF submitted to regulatory agencies in the US is known as a USDMF. Avacor and Mintop USDMF includes data on Avacor and Mintop's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Avacor and Mintop USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Avacor and Mintop suppliers with USDMF 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 Avacor and Mintop Drug Master File in Korea (Avacor and Mintop KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Avacor and Mintop. The MFDS reviews the Avacor and Mintop KDMF as part of the drug registration process and uses the information provided in the Avacor and Mintop KDMF to evaluate the safety and efficacy of the drug.
After submitting a Avacor and Mintop 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 Avacor and Mintop API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Avacor and Mintop suppliers with KDMF on PharmaCompass.
A Avacor and Mintop CEP of the European Pharmacopoeia monograph is often referred to as a Avacor and Mintop Certificate of Suitability (COS). The purpose of a Avacor and Mintop CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Avacor and Mintop EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Avacor and Mintop to their clients by showing that a Avacor and Mintop CEP has been issued for it. The manufacturer submits a Avacor and Mintop CEP (COS) as part of the market authorization procedure, and it takes on the role of a Avacor and Mintop CEP holder for the record. Additionally, the data presented in the Avacor and Mintop CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Avacor and Mintop DMF.
A Avacor and Mintop CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Avacor and Mintop 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 Avacor and Mintop suppliers with CEP (COS) on PharmaCompass.
A Avacor and Mintop written confirmation (Avacor and Mintop WC) is an official document issued by a regulatory agency to a Avacor and Mintop manufacturer, verifying that the manufacturing facility of a Avacor and Mintop active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Avacor and Mintop APIs or Avacor and Mintop finished pharmaceutical products to another nation, regulatory agencies frequently require a Avacor and Mintop WC (written confirmation) as part of the regulatory process.
click here to find a list of Avacor and Mintop 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 Avacor and Mintop as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Avacor and Mintop 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 Avacor and Mintop 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 Avacor and Mintop and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Avacor and Mintop NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Avacor and Mintop suppliers with NDC on PharmaCompass.
Avacor and Mintop 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 Avacor and Mintop 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 Avacor and Mintop GMP manufacturer or Avacor and Mintop GMP API supplier for your needs.
A Avacor and Mintop CoA (Certificate of Analysis) is a formal document that attests to Avacor and Mintop's compliance with Avacor and Mintop specifications and serves as a tool for batch-level quality control.
Avacor and Mintop CoA mostly includes findings from lab analyses of a specific batch. For each Avacor and Mintop 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.
Avacor and Mintop may be tested according to a variety of international standards, such as European Pharmacopoeia (Avacor and Mintop EP), Avacor and Mintop JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Avacor and Mintop USP).
