Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
01 1Pfanstiehl, Inc.
02 1Archimica S.p.A.
03 1Asahi Kasei Finechem Co., Ltd.
04 1Zhejiang Hisun Pharmaceutical Co., Ltd.
01 4Cytarabine
01 1China
02 1Italy
03 1Japan
04 1U.S.A
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
NDC Package Code : 67430-075
Start Marketing Date : 2017-01-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55512-0026
Start Marketing Date : 2019-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12848-1003
Start Marketing Date : 1986-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 58623-0026
Start Marketing Date : 2004-01-15
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 Cytarabine 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 Cytarabine manufacturer or Cytarabine supplier for your needs.
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PharmaCompass also assists you with knowing the Cytarabine API Price utilized in the formulation of products. Cytarabine API Price is not always fixed or binding as the Cytarabine Price is obtained through a variety of data sources. The Cytarabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytarabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytarabine, including repackagers and relabelers. The FDA regulates Cytarabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytarabine 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 Cytarabine supplier is an individual or a company that provides Cytarabine active pharmaceutical ingredient (API) or Cytarabine finished formulations upon request. The Cytarabine suppliers may include Cytarabine 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 Cytarabine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cytarabine 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 Cytarabine 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 Cytarabine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cytarabine NDC to their finished compounded human drug products, they may choose to do so.
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