DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1MSN Laboratories Private Limited
03 1Novartis Pharma AG@[Sieving Process] Novartis Pharma Stein AG
04 1PLIVA Croatia Ltd
05 1Sterling Pharma Ringaskiddy Limited@[Sieving Process]Novartis Pharma Stein AG
01 1Kukjeon Pharmaceutical Co., Ltd.
02 2Novartis Korea Ltd.
03 1Pami Future Co., Ltd.
04 1Samoh Pharmaceutical Co., Ltd.
01 1Nilotinib
02 1Nilotinib hydrochloride
03 3Nilotinib hydrochloride monohydrate
01 1Croatia
02 2India
03 1Switzerland
04 1United Kingdom
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Nilotinib hydrochloride monohydrate
Registrant Name : Pami Future Co., Ltd.
Registration Date : 2024-01-23
Registration Number : No. 574-23-ND
Manufacturer Name : Dr. Reddy's Laboratories Lim...
Manufacturer Address : CTO Unit-VI, APIIC Industrial Estate, Pydibhimavaram Village, Ranasthalam Mandal, Sri...
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2022-04-25
Registration Number : No. 173-36-ND
Manufacturer Name : MSN Laboratories Private Lim...
Manufacturer Address : (Unit-II), Sy.No.50, 53, 53/A, 54&54A, Kardanur (village), Patancheru (Mandal), Sanga...
Nilotinib hydrochloride monohydrate
Registrant Name : Novartis Korea Ltd.
Registration Date : 2007-12-04
Registration Number : Su163-9-ND
Manufacturer Name : Novartis Pharma AG@[Sieving ...
Manufacturer Address : Lichtstrasse 35, 4056 Basel, Switzerland@Schaffhauserstrasse, 4332 Stein, Switzerland
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2022-10-18
Registration Number : Number 207-57-ND
Manufacturer Name : PLIVA Croatia Ltd
Manufacturer Address : 10291 Prigorje Brdovecko, Prudnicka cesta 54, Republic of Croatia
Nilotinib hydrochloride monohydrate
Registrant Name : Novartis Korea Ltd.
Registration Date : 2015-02-09
Registration Number : Number 2554-12-ND
Manufacturer Name : Sterling Pharma Ringaskiddy ...
Manufacturer Address : Ringaskiddy, Cork, P43 FR63, Ireland@Schaffhauserstrasse, CH-4332 Stein, Switzerland
A Nilotinib hydrochloride anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nilotinib hydrochloride anhydrous, including repackagers and relabelers. The FDA regulates Nilotinib hydrochloride anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nilotinib hydrochloride anhydrous 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 anhydrous manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nilotinib hydrochloride anhydrous supplier is an individual or a company that provides Nilotinib hydrochloride anhydrous active pharmaceutical ingredient (API) or Nilotinib hydrochloride anhydrous finished formulations upon request. The Nilotinib hydrochloride anhydrous suppliers may include Nilotinib hydrochloride anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Nilotinib hydrochloride anhydrous 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 anhydrous Drug Master File in Korea (Nilotinib hydrochloride anhydrous KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nilotinib hydrochloride anhydrous. The MFDS reviews the Nilotinib hydrochloride anhydrous KDMF as part of the drug registration process and uses the information provided in the Nilotinib hydrochloride anhydrous KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nilotinib hydrochloride anhydrous 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 anhydrous API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nilotinib hydrochloride anhydrous suppliers with KDMF on PharmaCompass.
We have 5 companies offering Nilotinib hydrochloride anhydrous
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