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  • TABLET;ORAL - 150MG
  • TABLET;ORAL - 300MG
  • TABLET;ORAL - 600MG

Looking for 28721-07-5 / Oxcarbazepine API manufacturers, exporters & distributors?

Oxcarbazepine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Oxcarbazepine

Synonyms

28721-07-5, Trileptal, Oxcarbamazepine, Oxcarbazepina, Oxcarbazepinum, Gp 47680

Cas Number

28721-07-5

Unique Ingredient Identifier (UNII)

VZI5B1W380

About Oxcarbazepine

A carbamazepine derivative that acts as a voltage-gated sodium channel blocker. It is used for the treatment of PARTIAL SEIZURES with or without secondary generalization. It is also an inducer of CYTOCHROME P-450 CYP3A4.

AM20040094 Manufacturers

A AM20040094 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20040094, including repackagers and relabelers. The FDA regulates AM20040094 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20040094 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 AM20040094 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

AM20040094 Suppliers

A AM20040094 supplier is an individual or a company that provides AM20040094 active pharmaceutical ingredient (API) or AM20040094 finished formulations upon request. The AM20040094 suppliers may include AM20040094 API manufacturers, exporters, distributors and traders.

click here to find a list of AM20040094 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

AM20040094 USDMF

A AM20040094 DMF (Drug Master File) is a document detailing the whole manufacturing process of AM20040094 active pharmaceutical ingredient (API) in detail. Different forms of AM20040094 DMFs exist exist since differing nations have different regulations, such as AM20040094 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A AM20040094 DMF submitted to regulatory agencies in the US is known as a USDMF. AM20040094 USDMF includes data on AM20040094's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AM20040094 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of AM20040094 suppliers with USDMF on PharmaCompass.

AM20040094 KDMF

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

Pharmaceutical companies submit a AM20040094 Drug Master File in Korea (AM20040094 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AM20040094. The MFDS reviews the AM20040094 KDMF as part of the drug registration process and uses the information provided in the AM20040094 KDMF to evaluate the safety and efficacy of the drug.

After submitting a AM20040094 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 AM20040094 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of AM20040094 suppliers with KDMF on PharmaCompass.

AM20040094 CEP

A AM20040094 CEP of the European Pharmacopoeia monograph is often referred to as a AM20040094 Certificate of Suitability (COS). The purpose of a AM20040094 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AM20040094 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AM20040094 to their clients by showing that a AM20040094 CEP has been issued for it. The manufacturer submits a AM20040094 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AM20040094 CEP holder for the record. Additionally, the data presented in the AM20040094 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AM20040094 DMF.

A AM20040094 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AM20040094 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 AM20040094 suppliers with CEP (COS) on PharmaCompass.

AM20040094 WC

A AM20040094 written confirmation (AM20040094 WC) is an official document issued by a regulatory agency to a AM20040094 manufacturer, verifying that the manufacturing facility of a AM20040094 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AM20040094 APIs or AM20040094 finished pharmaceutical products to another nation, regulatory agencies frequently require a AM20040094 WC (written confirmation) as part of the regulatory process.

click here to find a list of AM20040094 suppliers with Written Confirmation (WC) on PharmaCompass.

AM20040094 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 AM20040094 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for AM20040094 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 AM20040094 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 AM20040094 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AM20040094 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of AM20040094 suppliers with NDC on PharmaCompass.

AM20040094 GMP

AM20040094 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 AM20040094 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 AM20040094 GMP manufacturer or AM20040094 GMP API supplier for your needs.

AM20040094 CoA

A AM20040094 CoA (Certificate of Analysis) is a formal document that attests to AM20040094's compliance with AM20040094 specifications and serves as a tool for batch-level quality control.

AM20040094 CoA mostly includes findings from lab analyses of a specific batch. For each AM20040094 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.

AM20040094 may be tested according to a variety of international standards, such as European Pharmacopoeia (AM20040094 EP), AM20040094 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AM20040094 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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