Market Place
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations. 
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01 Dr. Reddy's Laboratories Limited (1)
02 MSN Laboratories Private Limited (1)
03 Novartis Pharma AG@[sieving process] Novartis Pharma Stein AG (1)
04 PLIVA Croatia Ltd (1)
05 Sterling Pharma Ringaskiddy Limited@[Sifting Process]Novartis Pharma Stein AG (1)
01 Farmirae Co., Ltd. (1)
02 Kookjeon Pharmaceutical Co., Ltd. (1)
03 Novartis Korea Co., Ltd. (2)
04 Samo Pharmaceutical Co., Ltd. (1)
01 Nilotinib (1)
02 Nilotinib hydrochloride (1)
03 Nilotinib hydrochloride monohydrate (3)
01 Croatia (1)
02 India (2)
03 Switzerland (2)
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PharmaCompass offers a list of Nilotinib 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 Nilotinib manufacturer or Nilotinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nilotinib manufacturer or Nilotinib supplier.
PharmaCompass also assists you with knowing the Nilotinib API Price utilized in the formulation of products. Nilotinib API Price is not always fixed or binding as the Nilotinib Price is obtained through a variety of data sources. The Nilotinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A nilotinib hydrochloride dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nilotinib hydrochloride dihydrate, including repackagers and relabelers. The FDA regulates nilotinib hydrochloride dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nilotinib hydrochloride dihydrate 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 nilotinib hydrochloride dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A nilotinib hydrochloride dihydrate supplier is an individual or a company that provides nilotinib hydrochloride dihydrate active pharmaceutical ingredient (API) or nilotinib hydrochloride dihydrate finished formulations upon request. The nilotinib hydrochloride dihydrate suppliers may include nilotinib hydrochloride dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of nilotinib hydrochloride dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a nilotinib hydrochloride dihydrate Drug Master File in Korea (nilotinib hydrochloride dihydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of nilotinib hydrochloride dihydrate. The MFDS reviews the nilotinib hydrochloride dihydrate KDMF as part of the drug registration process and uses the information provided in the nilotinib hydrochloride dihydrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a nilotinib hydrochloride dihydrate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their nilotinib hydrochloride dihydrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of nilotinib hydrochloride dihydrate suppliers with KDMF on PharmaCompass.
We have 4 companies offering nilotinib hydrochloride dihydrate
Get in contact with the supplier of your choice:
