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Looking for 95-25-0 / Chlorzoxazone API manufacturers, exporters & distributors?

Chlorzoxazone manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Chlorzoxazone

Synonyms

95-25-0, Paraflex, Chloroxazone, Chlorzoxazon, 5-chloro-2-benzoxazolone, 5-chloro-2-benzoxazolinone

Cas Number

95-25-0

Unique Ingredient Identifier (UNII)

H0DE420U8G

About Chlorzoxazone

A centrally acting central muscle relaxant with sedative properties. It is claimed to inhibit muscle spasm by exerting an effect primarily at the level of the spinal cord and subcortical areas of the brain. (From Martindale, The Extra Pharmacopoea, 30th ed, p1202)

MolPort-001-759-947 Manufacturers

A MolPort-001-759-947 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-759-947, including repackagers and relabelers. The FDA regulates MolPort-001-759-947 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-759-947 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 MolPort-001-759-947 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-759-947 Suppliers

A MolPort-001-759-947 supplier is an individual or a company that provides MolPort-001-759-947 active pharmaceutical ingredient (API) or MolPort-001-759-947 finished formulations upon request. The MolPort-001-759-947 suppliers may include MolPort-001-759-947 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-759-947 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-759-947 USDMF

A MolPort-001-759-947 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-759-947 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-759-947 DMFs exist exist since differing nations have different regulations, such as MolPort-001-759-947 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-759-947 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-759-947 USDMF includes data on MolPort-001-759-947's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-759-947 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-759-947 suppliers with USDMF on PharmaCompass.

MolPort-001-759-947 KDMF

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

Pharmaceutical companies submit a MolPort-001-759-947 Drug Master File in Korea (MolPort-001-759-947 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MolPort-001-759-947. The MFDS reviews the MolPort-001-759-947 KDMF as part of the drug registration process and uses the information provided in the MolPort-001-759-947 KDMF to evaluate the safety and efficacy of the drug.

After submitting a MolPort-001-759-947 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 MolPort-001-759-947 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of MolPort-001-759-947 suppliers with KDMF on PharmaCompass.

MolPort-001-759-947 WC

A MolPort-001-759-947 written confirmation (MolPort-001-759-947 WC) is an official document issued by a regulatory agency to a MolPort-001-759-947 manufacturer, verifying that the manufacturing facility of a MolPort-001-759-947 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MolPort-001-759-947 APIs or MolPort-001-759-947 finished pharmaceutical products to another nation, regulatory agencies frequently require a MolPort-001-759-947 WC (written confirmation) as part of the regulatory process.

click here to find a list of MolPort-001-759-947 suppliers with Written Confirmation (WC) on PharmaCompass.

MolPort-001-759-947 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 MolPort-001-759-947 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-759-947 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 MolPort-001-759-947 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 MolPort-001-759-947 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-759-947 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-759-947 suppliers with NDC on PharmaCompass.

MolPort-001-759-947 GMP

MolPort-001-759-947 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 MolPort-001-759-947 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 MolPort-001-759-947 GMP manufacturer or MolPort-001-759-947 GMP API supplier for your needs.

MolPort-001-759-947 CoA

A MolPort-001-759-947 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-759-947's compliance with MolPort-001-759-947 specifications and serves as a tool for batch-level quality control.

MolPort-001-759-947 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-759-947 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.

MolPort-001-759-947 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-759-947 EP), MolPort-001-759-947 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-759-947 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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