01 1Siegfried AG
02 1Zoetis Inc.
01 1Oclacitinib Maleate
02 1Oclacitinib maleate
01 1Switzerland
02 1U.S.A
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
NDC Package Code : 54771-1344
Start Marketing Date : 2020-03-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Oclacitinib Maleate 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 Maleate manufacturer or Oclacitinib Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oclacitinib Maleate manufacturer or Oclacitinib Maleate supplier.
PharmaCompass also assists you with knowing the Oclacitinib Maleate API Price utilized in the formulation of products. Oclacitinib Maleate API Price is not always fixed or binding as the Oclacitinib Maleate Price is obtained through a variety of data sources. The Oclacitinib Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oclacitinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oclacitinib, including repackagers and relabelers. The FDA regulates Oclacitinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oclacitinib 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 Oclacitinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oclacitinib supplier is an individual or a company that provides Oclacitinib active pharmaceutical ingredient (API) or Oclacitinib finished formulations upon request. The Oclacitinib suppliers may include Oclacitinib API manufacturers, exporters, distributors and traders.
click here to find a list of Oclacitinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oclacitinib 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 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 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oclacitinib NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oclacitinib suppliers with NDC on PharmaCompass.
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