Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Metrochem API Private Limited
03 1MSN Life Sciences Private Limited
01 1STIRIPENTOL
02 2Stiripentol
01 3India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-069
Start Marketing Date : 2024-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
NDC Package Code : 42765-058
Start Marketing Date : 2023-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-075
Start Marketing Date : 2019-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Stiripentol 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 Stiripentol manufacturer or Stiripentol supplier for your needs.
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PharmaCompass also assists you with knowing the Stiripentol API Price utilized in the formulation of products. Stiripentol API Price is not always fixed or binding as the Stiripentol Price is obtained through a variety of data sources. The Stiripentol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diacomit reg manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diacomit reg, including repackagers and relabelers. The FDA regulates Diacomit reg manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diacomit reg API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Diacomit reg supplier is an individual or a company that provides Diacomit reg active pharmaceutical ingredient (API) or Diacomit reg finished formulations upon request. The Diacomit reg suppliers may include Diacomit reg API manufacturers, exporters, distributors and traders.
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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 Diacomit reg as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diacomit reg 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 Diacomit reg 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 Diacomit reg and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diacomit reg NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diacomit reg suppliers with NDC on PharmaCompass.
We have 3 companies offering Diacomit reg
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