01 1Hetero Labs Limited
02 1MSN Laboratories Private Limited
03 1Medichem Manufacturing (Malta) Ltd.
04 1Medichem S.A.
05 1Pfizer Asia Manufacturing Pte Ltd
06 1SHILPA PHARMA LIFESCIENCES LIMITED
07 1Sicor S.r.l.
01 6Sunitinib Malate
02 1sunitinib malate
01 3India
02 1Italy
03 2Spain
04 1U.S.A
NDC Package Code : 68554-0078
Start Marketing Date : 2006-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53296-0091
Start Marketing Date : 2010-06-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 16436-0091
Start Marketing Date : 2010-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0081
Start Marketing Date : 2018-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68724-1234
Start Marketing Date : 2019-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82920-037
Start Marketing Date : 2023-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53183-4012
Start Marketing Date : 2018-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sunitinib 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 Sunitinib manufacturer or Sunitinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sunitinib manufacturer or Sunitinib supplier.
PharmaCompass also assists you with knowing the Sunitinib API Price utilized in the formulation of products. Sunitinib API Price is not always fixed or binding as the Sunitinib Price is obtained through a variety of data sources. The Sunitinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sutent (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sutent (TN), including repackagers and relabelers. The FDA regulates Sutent (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sutent (TN) 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 Sutent (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sutent (TN) supplier is an individual or a company that provides Sutent (TN) active pharmaceutical ingredient (API) or Sutent (TN) finished formulations upon request. The Sutent (TN) suppliers may include Sutent (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Sutent (TN) 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 Sutent (TN) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sutent (TN) 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 Sutent (TN) 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 Sutent (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sutent (TN) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sutent (TN) suppliers with NDC on PharmaCompass.
We have 6 companies offering Sutent (TN)
Get in contact with the supplier of your choice:
