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Parand Darou Oxycodone Hydrochloride Parand Darou Oxycodone Hydrochloride

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  • CAPSULE;ORAL - 5MG
  • SOLUTION;ORAL - 100MG/5ML
  • SOLUTION;ORAL - 5MG/5ML
  • TABLET;ORAL - 5MG
  • TABLET;ORAL - 7.5MG
  • TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 13.5MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 18MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 27MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 36MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 9MG
  • TABLET, EXTENDED RELEASE;ORAL - 10MG
  • TABLET, EXTENDED RELEASE;ORAL - 15MG
  • TABLET, EXTENDED RELEASE;ORAL - 20MG
  • TABLET, EXTENDED RELEASE;ORAL - 30MG
  • TABLET, EXTENDED RELEASE;ORAL - 40MG
  • TABLET, EXTENDED RELEASE;ORAL - 60MG
  • TABLET, EXTENDED RELEASE;ORAL - 80MG
  • TABLET;ORAL - 325MG;5MG

Looking for 124-90-3 / Oxycodone Hydrochloride API manufacturers, exporters & distributors?

Oxycodone Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Oxycodone 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 Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier.

PharmaCompass also assists you with knowing the Oxycodone Hydrochloride API Price utilized in the formulation of products. Oxycodone Hydrochloride API Price is not always fixed or binding as the Oxycodone Hydrochloride Price is obtained through a variety of data sources. The Oxycodone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Oxycodone Hydrochloride

Synonyms

124-90-3, Oxycodone hcl, Oxecta, Oxycontin, Endocodone, Roxicodone

Cas Number

124-90-3

Unique Ingredient Identifier (UNII)

C1ENJ2TE6C

About Oxycodone Hydrochloride

A semisynthetic derivative of CODEINE.

Oxycodone Hydrochloride Manufacturers

A Oxycodone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxycodone Hydrochloride, including repackagers and relabelers. The FDA regulates Oxycodone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxycodone 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 Oxycodone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Oxycodone Hydrochloride Suppliers

A Oxycodone Hydrochloride supplier is an individual or a company that provides Oxycodone Hydrochloride active pharmaceutical ingredient (API) or Oxycodone Hydrochloride finished formulations upon request. The Oxycodone Hydrochloride suppliers may include Oxycodone Hydrochloride API manufacturers, exporters, distributors and traders.

click here to find a list of Oxycodone Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Oxycodone Hydrochloride USDMF

A Oxycodone Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxycodone Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Oxycodone Hydrochloride DMFs exist exist since differing nations have different regulations, such as Oxycodone Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Oxycodone Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Oxycodone Hydrochloride USDMF includes data on Oxycodone Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxycodone Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Oxycodone Hydrochloride suppliers with USDMF on PharmaCompass.

Oxycodone Hydrochloride JDMF

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 Hydrochloride Drug Master File in Japan (Oxycodone Hydrochloride JDMF) empowers Oxycodone 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 Oxycodone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Oxycodone 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 Oxycodone Hydrochloride suppliers with JDMF on PharmaCompass.

Oxycodone Hydrochloride KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Oxycodone Hydrochloride Drug Master File in Korea (Oxycodone Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Oxycodone Hydrochloride. The MFDS reviews the Oxycodone Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Oxycodone Hydrochloride KDMF to evaluate the safety and efficacy of the drug.

After submitting a Oxycodone Hydrochloride 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 Hydrochloride API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Oxycodone Hydrochloride suppliers with KDMF on PharmaCompass.

Oxycodone Hydrochloride CEP

A Oxycodone Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Oxycodone Hydrochloride Certificate of Suitability (COS). The purpose of a Oxycodone Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxycodone Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxycodone Hydrochloride to their clients by showing that a Oxycodone Hydrochloride CEP has been issued for it. The manufacturer submits a Oxycodone Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxycodone Hydrochloride CEP holder for the record. Additionally, the data presented in the Oxycodone Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxycodone Hydrochloride DMF.

A Oxycodone Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxycodone 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 Oxycodone Hydrochloride suppliers with CEP (COS) on PharmaCompass.

Oxycodone Hydrochloride WC

A Oxycodone Hydrochloride written confirmation (Oxycodone Hydrochloride WC) is an official document issued by a regulatory agency to a Oxycodone Hydrochloride manufacturer, verifying that the manufacturing facility of a Oxycodone Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxycodone Hydrochloride APIs or Oxycodone Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxycodone Hydrochloride WC (written confirmation) as part of the regulatory process.

click here to find a list of Oxycodone Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.

Oxycodone Hydrochloride NDC

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 Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Oxycodone Hydrochloride API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Oxycodone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxycodone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Oxycodone Hydrochloride suppliers with NDC on PharmaCompass.

Oxycodone Hydrochloride GMP

Oxycodone 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 Oxycodone 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 Oxycodone Hydrochloride GMP manufacturer or Oxycodone Hydrochloride GMP API supplier for your needs.

Oxycodone Hydrochloride CoA

A Oxycodone Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Oxycodone Hydrochloride's compliance with Oxycodone Hydrochloride specifications and serves as a tool for batch-level quality control.

Oxycodone Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Oxycodone 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.

Oxycodone Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxycodone Hydrochloride EP), Oxycodone Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxycodone Hydrochloride USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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