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API SUPPLIERS
Veranova: A CDMO that manages complexity with confidence.
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Parand Darou is a knowledge-based company, focused on the production of Narcotic APIs.
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Temad- We think of world-class quality.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
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KDMF
Veranova: A CDMO that manages complexity with confidence.
NDC
KDMF
ROW, CN
Veranova: A CDMO that manages complexity with confidence.
NDC
KDMF
ROW, CN
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
CEP/COS
NDC
KDMF
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USDMF
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Drugs in Development
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DOSAGE - CAPSULE;ORAL - 5MG
USFDA APPLICATION NUMBER - 200534
DOSAGE - SOLUTION;ORAL - 100MG/5ML
USFDA APPLICATION NUMBER - 200535
DOSAGE - SOLUTION;ORAL - 5MG/5ML
USFDA APPLICATION NUMBER - 200535
DOSAGE - SOLUTION;ORAL - 5MG/5ML
USFDA APPLICATION NUMBER - 201194
DOSAGE - TABLET;ORAL - 5MG
USFDA APPLICATION NUMBER - 202080
DOSAGE - TABLET;ORAL - 7.5MG
USFDA APPLICATION NUMBER - 202080
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 325M...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 204031
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 13....DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 13.5MG
USFDA APPLICATION NUMBER - 208090
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 18M...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 18MG
USFDA APPLICATION NUMBER - 208090
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 27M...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 27MG
USFDA APPLICATION NUMBER - 208090
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 36M...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 36MG
USFDA APPLICATION NUMBER - 208090
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 9MG
USFDA APPLICATION NUMBER - 208090
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 10MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 15MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 20MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 30MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 40MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 60MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 80MG
USFDA APPLICATION NUMBER - 22272
DOSAGE - TABLET;ORAL - 325MG;5MG
USFDA APPLICATION NUMBER - 87003
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ABOUT THIS PAGE
A Oxycodone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxycodone, including repackagers and relabelers. The FDA regulates Oxycodone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxycodone 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 Oxycodone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxycodone supplier is an individual or a company that provides Oxycodone active pharmaceutical ingredient (API) or Oxycodone finished formulations upon request. The Oxycodone suppliers may include Oxycodone API manufacturers, exporters, distributors and traders.
click here to find a list of Oxycodone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxycodone DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxycodone active pharmaceutical ingredient (API) in detail. Different forms of Oxycodone DMFs exist exist since differing nations have different regulations, such as Oxycodone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxycodone DMF submitted to regulatory agencies in the US is known as a USDMF. Oxycodone USDMF includes data on Oxycodone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxycodone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxycodone 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 Oxycodone Drug Master File in Japan (Oxycodone JDMF) empowers Oxycodone 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 Oxycodone JDMF during the approval evaluation for pharmaceutical products. At the time of Oxycodone 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 Oxycodone 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 Oxycodone Drug Master File in Korea (Oxycodone KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Oxycodone. The MFDS reviews the Oxycodone KDMF as part of the drug registration process and uses the information provided in the Oxycodone KDMF to evaluate the safety and efficacy of the drug.
After submitting a Oxycodone 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 Oxycodone API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Oxycodone suppliers with KDMF on PharmaCompass.
A Oxycodone CEP of the European Pharmacopoeia monograph is often referred to as a Oxycodone Certificate of Suitability (COS). The purpose of a Oxycodone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxycodone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxycodone to their clients by showing that a Oxycodone CEP has been issued for it. The manufacturer submits a Oxycodone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxycodone CEP holder for the record. Additionally, the data presented in the Oxycodone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxycodone DMF.
A Oxycodone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxycodone 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 Oxycodone suppliers with CEP (COS) on PharmaCompass.
A Oxycodone written confirmation (Oxycodone WC) is an official document issued by a regulatory agency to a Oxycodone manufacturer, verifying that the manufacturing facility of a Oxycodone active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxycodone APIs or Oxycodone finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxycodone WC (written confirmation) as part of the regulatory process.
click here to find a list of Oxycodone 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 Oxycodone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxycodone 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 Oxycodone 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 Oxycodone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxycodone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxycodone suppliers with NDC on PharmaCompass.
Oxycodone 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 Oxycodone 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 Oxycodone GMP manufacturer or Oxycodone GMP API supplier for your needs.
A Oxycodone CoA (Certificate of Analysis) is a formal document that attests to Oxycodone's compliance with Oxycodone specifications and serves as a tool for batch-level quality control.
Oxycodone CoA mostly includes findings from lab analyses of a specific batch. For each Oxycodone 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.
Oxycodone may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxycodone EP), Oxycodone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxycodone USP).
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