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Looking for 59-63-2 / Isocarboxazid API manufacturers, exporters & distributors?

Isocarboxazid manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Isocarboxazid

Synonyms

59-63-2, Isocarboxazide, Marplan, Enerzer, N'-benzyl-5-methylisoxazole-3-carbohydrazide, Isocarbonazid

Cas Number

59-63-2

Unique Ingredient Identifier (UNII)

34237V843T

About Isocarboxazid

An MAO inhibitor that is effective in the treatment of major depression, dysthymic disorder, and atypical depression. It also is useful in the treatment of panic disorder and the phobic disorders. (From AMA, Drug Evaluations Annual, 1994, p311)

Isocarboxazid Manufacturers

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

Isocarboxazid Suppliers

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

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

Isocarboxazid USDMF

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

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

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

Isocarboxazid 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 Isocarboxazid as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Isocarboxazid GMP

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

Isocarboxazid CoA

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

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

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