01 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
02 1RAVI BIOLIFE PRIVATE LTD. Mumbai IN
03 1SHANDONG LIXIN PHARMACEUTICAL CO. LTD. Zibo CN
01 3Nilotinib hydrochloride monohydrate
01 1China
02 1India
03 1Blank
01 3Valid
Nilotinib Hydrochloride Monohydrate
Certificate Number : R0-CEP 2020-176 - Rev 00
Status : Valid
Issue Date : 2022-12-06
Type : Chemical
Substance Number : 2993
Nilotinib Hydrochloride Monohydrate
Certificate Number : R0-CEP 2021-133 - Rev 00
Status : Valid
Issue Date : 2023-07-21
Type : Chemical
Substance Number : 2993
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Nilotinib Hydrochloride Monohydrate
Certificate Number : CEP 2022-425 - Rev 00
Status : Valid
Issue Date : 2024-04-19
Type : Chemical
Substance Number : 2993
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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.
A Nilotinib hydrochloride anhydrous CEP of the European Pharmacopoeia monograph is often referred to as a Nilotinib hydrochloride anhydrous Certificate of Suitability (COS). The purpose of a Nilotinib hydrochloride anhydrous CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nilotinib hydrochloride anhydrous EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nilotinib hydrochloride anhydrous to their clients by showing that a Nilotinib hydrochloride anhydrous CEP has been issued for it. The manufacturer submits a Nilotinib hydrochloride anhydrous CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nilotinib hydrochloride anhydrous CEP holder for the record. Additionally, the data presented in the Nilotinib hydrochloride anhydrous CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nilotinib hydrochloride anhydrous DMF.
A Nilotinib hydrochloride anhydrous CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nilotinib hydrochloride anhydrous CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Nilotinib hydrochloride anhydrous suppliers with CEP (COS) on PharmaCompass.
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