01 1Siegfried AG
01 1Oclacitinib Maleate
01 1Switzerland
NDC Package Code : 17205-097
Start Marketing Date : 2019-04-12
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 Oclacitinib 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 Oclacitinib manufacturer or Oclacitinib supplier for your needs.
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PharmaCompass also assists you with knowing the Oclacitinib API Price utilized in the formulation of products. Oclacitinib API Price is not always fixed or binding as the Oclacitinib Price is obtained through a variety of data sources. The Oclacitinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oclacitinib Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oclacitinib Maleate, including repackagers and relabelers. The FDA regulates Oclacitinib Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oclacitinib Maleate 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 Oclacitinib Maleate supplier is an individual or a company that provides Oclacitinib Maleate active pharmaceutical ingredient (API) or Oclacitinib Maleate finished formulations upon request. The Oclacitinib Maleate suppliers may include Oclacitinib Maleate 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 Oclacitinib Maleate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oclacitinib Maleate 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 Oclacitinib Maleate 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 Oclacitinib Maleate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oclacitinib Maleate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oclacitinib Maleate suppliers with NDC on PharmaCompass.
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