Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co., Ltd.
02 1DOTTIKON EXCLUSIVE SYNTHESIS AG
03 1MSN Laboratories Private Limited
01 1Selumetinib Hyd Sulfate
02 2Selumetinib Sulfate
01 1India
02 1Switzerland
03 1Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6278
Start Marketing Date : 2023-07-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54864-874
Start Marketing Date : 2020-04-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0523
Start Marketing Date : 2026-03-28
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Selumetinib API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Selumetinib manufacturer or Selumetinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selumetinib manufacturer or Selumetinib supplier.
A Selumetinib Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selumetinib Sulfate, including repackagers and relabelers. The FDA regulates Selumetinib Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selumetinib Sulfate 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 Selumetinib Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Selumetinib Sulfate supplier is an individual or a company that provides Selumetinib Sulfate active pharmaceutical ingredient (API) or Selumetinib Sulfate finished formulations upon request. The Selumetinib Sulfate suppliers may include Selumetinib Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Selumetinib Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Selumetinib Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Selumetinib Sulfate 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 Selumetinib Sulfate 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 Selumetinib Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Selumetinib Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Selumetinib Sulfate suppliers with NDC on PharmaCompass.
We have 3 companies offering Selumetinib Sulfate
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