01 1HETERO LABS LIMITED
02 1MSN Laboratories Private Limited
03 1Pfizer Asia Manufacturing Pte Ltd
04 1Pfizer Ireland Pharmaceuticals Unlimited Company
01 4Crizotinib
01 2India
02 2U.S.A
NDC Package Code : 68554-0170
Start Marketing Date : 2011-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0501
Start Marketing Date : 2023-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60715-1551
Start Marketing Date : 2023-10-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68724-1020
Start Marketing Date : 2018-05-24
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 Crizotinib 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 Crizotinib manufacturer or Crizotinib supplier for your needs.
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PharmaCompass also assists you with knowing the Crizotinib API Price utilized in the formulation of products. Crizotinib API Price is not always fixed or binding as the Crizotinib Price is obtained through a variety of data sources. The Crizotinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SB431542, SB 431542 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SB431542, SB 431542, including repackagers and relabelers. The FDA regulates SB431542, SB 431542 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SB431542, SB 431542 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 SB431542, SB 431542 supplier is an individual or a company that provides SB431542, SB 431542 active pharmaceutical ingredient (API) or SB431542, SB 431542 finished formulations upon request. The SB431542, SB 431542 suppliers may include SB431542, SB 431542 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 SB431542, SB 431542 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for SB431542, SB 431542 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 SB431542, SB 431542 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 SB431542, SB 431542 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a SB431542, SB 431542 NDC to their finished compounded human drug products, they may choose to do so.
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We have 3 companies offering SB431542, SB 431542
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